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عضویت

جستجوی مقالات مرتبط با کلیدواژه « Clinical Presentation » در نشریات گروه « پزشکی »

  • Kalsoom Akhlaq, Hadi Khan, Zafar Ali, Muslim Atiq *, Shahzad Riyaz, Umar Raja, Amen Kiani
    Background

    Pancreatic neuroendocrine tumors (P-NETs) constitute a subset of pancreatic mass lesions characterized by diverse clinical presentations. Despite their inherent malignant potential, the timely identification and treatment of these tumors are critical for achieving favorable clinical outcomes. This study aims to shed light on the heterogeneous tumor biology of P-NETs and the management strategies employed at a tertiary care center in Pakistan.

    Method

    A retrospective study encompassing all patients with a biopsy-confirmed diagnosis of P-NETs at Shifa International Hospital between January 1st, 2016, and June 30th, 2021, was conducted. Meticulous data extraction from pathology records and thorough searches of medical records were performed to gather relevant demographic and clinical information.

    Results

    A total of 24 patients were retrieved from our database, with 13 (54%) female patients. The mean age was 49.5 ± 16.3 years. Eight out of the 24 patients presented with abdominal pain. Most patients (14 out of 24) had lesions in the pancreatic head region. In three cases, lesions exhibited multicentricity. The mean lesion size measured 4.4 ± 2.3 cm. Three of the 24 patients displayed distant liver metastasis at the presentation time. 19 out of the 24 patients underwent surgical resections, while endoscopic ultrasound (EUS)-guided biopsy was performed in 4 out of 24 cases. EUS-guided tissue biopsy yielded accurate diagnoses in all four cases.

    Conclusion

    Most P-NETs are non-functional, and there is an almost equal distribution between male and female patients. Solitary lesions predominate, and metastasis is uncommon at initial presentation. EUS-guided fine needle biopsy stands out as a dependable diagnostic modality for P-NETs.

    Keywords: Neuroendocrine Tumors, Pancreas, Clinical presentation, Management, diagnosis}
  • Masoumeh Rezvani, MohammadTaghi Moghadamnia, Ehsan Kazemnejad Leili, Majid Pourshaikhian*, Hojjat Houshyari Khah
    Introduction

    The most important diagnostic indicator of Acute Coronary Syndrome (ACS) is typical clinical symptoms, like chest pain, but many patients may experience nonspecific (atypical) symptoms. Understanding these symptoms and their associated factors results in early diagnosis and more appropriate treatments.

    Objective

    We aimed to determine atypical clinical symptoms and their predictors in patients with Acute Coronary Syndrome.

    Materials and Methods

    This cross-sectional study was conducted on 1167 patients with ACS hospitalized at a specialized hospital in Rasht City, Iran, between December 2019 and October 2020. The research samples were selected by a consecutive sampling method. Data were collected through a researcher-made questionnaire by interview, in which sociodemographic characteristics, risk factors, disease-related factors, and symptoms of patients with ACS were collected. Data analysis was done by descriptive statistics and multiple logistic regression by the backward LR (likelihood ratio) method. The significance level was set as P<0.05.

    Results

    In this study, 56.3% of the patients were male. The Mean±SD age of the patients was 60.9±11.1 years. About 28.1% of the patients experienced atypical clinical symptoms. The most common atypical symptoms were shortness of breath (29.4%), back pain (18.3%), and left shoulder pain (12.7%). The predictors of atypical symptoms were age (OR=0.98, 95% CI; 0.975 - 0.999, P=0.047), alcohol use (OR=1.86, 95% CI; 1.047 - 3.303, P=0.034), brain diseases (OR=2.36, 95% CI; 1.463 - 3.811, P=0.001), blood diseases (OR=1.45, 95% CI; 1.059 - 2.002, P=0.021), and gastroesophageal reflux (OR=1.31, 95% CI; 1.006 - 1.719, P=0.045)

    Conclusion

    Since more than a quarter of ACS patients have unusual symptoms, detecting these symptoms and related factors can help in early diagnosis and conduct more appropriate medical treatment.

    Keywords: Acute coronary syndrome, Signs, symptoms, Clinical presentation}
  • setareh Akhavan, Jilah Agah, Elham Navipour
    Background

     Ovarian tumors are mostly detected in advanced stages. Early diagnosis of malignant ovarian germ cell tumors is so vital to keep life and fertility of the patients. We aimed to find out different presentations of malignant ovarian germ cell tumors based on age, parity and histology to help early diagnosis of the tumors. 

    Methods

     In this study, malignant ovarian germ cell tumors admitted in a referral center of gynecology oncology were studied 2001-2018. The symptoms and signs of the patients were collected and analyzed according to age, parity and specific histology. 

    Results

     128 cases of malignant germ cell tumors were detected. The primary symptoms included abdominal distension (45%), acute pain (40.95%), chronic pain (23.95%), menstrual irregularity (14.7%), sense of abdominal firmness and mass (7.72%), nausea (5.4%), fever (5.4%), lack of appetite (4.63%), virilization (3.1%), depletion of weight (3.1%), and 9.27% detected incidentally. Abdominal distension, and acute pain decreased after 24. Menstrual disorders and incidental detection in multiparas were significantly more than nulliparous (p<0.05). Abdominal distension was the prominent sign in dysgerminomas (50%). Almost 45% of immature, yolk sac, and mixed tumors referred with acute abdominal pain. The data showed that 85% of the patients had been suffering from some discomforts for days to months prior to the diagnosis. 

    Conclusion

     The majority of cases are symptomatic for a long time before the first visit although aging and parity can lessen their severity. Late diagnosis can lead to acute abdomen in some histology types. Young women and health providers should be warned about concerned presentations of ovarian tumors.

    Keywords: Clinical presentation, Germ cells, Histology, Ovary, Parity}
  • Larysa Kostyuchenko, Ihor Hrytsiuk, Yaryna Romanyshyn, Yaryna Boyko, Inga Sakovich
    Background

    APECED is a rare autosomal recessive disease, caused by mutations in the AIRE-gene resulting in a failure of T-cell tolerance, clinically characterized by multiple autoimmunopathies. The objective of the study was to determine the clinical and genetic features and consequences of APECED in a single-centre Ukrainian cohort of patients.

    Material and methods

    Out of five families, eight patients with APECED were included in the study. Family history and clinical information of each patient was collected; laboratory studies aimed at identifying endocrine disorders, other autoimmunity, and infections was done. Genetic testing by NGS was performed in four out of five families. Patients were included in the study after the written informed consent had been signed by their parents/legal guardians.

    Results

    In most patients, the onset of the disease was noted in childhood with manifestations of hypoparathyroidism and/or candidiasis. Adrenal insufficiency was associated later. Diabetes mellitus, hypothyroidism and hypogonadism were observed as other endocrinopathies. Five of eight patients (62.5%) developed autoimmune hepatitis, two patients suffered from autoimmune lung lesions, and two developed enteropathy. Two patients were diagnosed with brain damage: psychosis and autoimmune encephalitis. All the patients that we examined were homozygous carriers of the Finn major mutation R257X (c.769C> T) of the AIRE gene.

    Conclusion

    One or two endocrinopathies in combination with recurrent candidiasis are the key to a diagnosis of APECED. Most patients also develop organ autoimmunopathy. The mutation R257X (c.769C> T) of the AIRE-gene is predominant in the population of western Ukraine.

    Keywords: Polyendocrinopathies, APS-1, Autoimmune Encephalitis, Clinical Presentation}
  • Sedigheh Rafiei Tabatabaei, Minoo Fallahi *, Abbas Boskabadi, Naeeme Taslimi Taleghani, Fatemeh Pajouhandeh, Shahrzad Tabatabaee, Mitra Radfar, Shamsollah Nouripour, Mohammad Kazemian
    Introduction

    The Novel coronavirus, sars-cov-2, is responsible for the recent pandemic. Although it mostly affects adults, children of all ages, including neonates, can become ill with Covid-19, as well. The real prevalence rate of coronavirus disease 2019 (COVID-19) in children is unknown. However, the severity of symptoms in children and neonates is less than in adults. Regarding the new presentation of this disease, the current study has reported a case series of COVID-19 in neonates.

    Case Presentation

    In this article, 10 neonates with COVID- 19 admitted to our neonatal intensive care units are reported. All reported neonates had general suspicious symptoms of COVID- 19 with positive results for SARS-CoV-2 assessed by polymerase chain reaction (PCR) from the nasopharynx area or nose of the patients. All neonates, except for two of them, were term neonates. One case had open-heart surgery for congenital heart disease (transposition of the great arteries (TGA)). The mean patients age was 7.8 days on admission. The most frequent symptom was fever. Severe respiratory symptoms were reported in two cases. Also, abnormal radiologic findings in the chest X-ray were detected in two cases. Regarding the lack of significant respiratory symptoms in most of the patients, the lung computed tomography (CT) scan was taken just from one neonate. Leukopenia (WBC < 5000/mm3) was detected in one case, with no lymphopenia in all neonates. The positive C-reactive protein test was not found in all cases. No patient was treated by special anti-viral agents for COVID-19, and usual antibiotic treatment for neonatal sepsis was administered for all cases. All patients, except for one, survived with no significant sequela of the disease.

    Conclusions

    This study demonstrated that clinical manifestations, as well as laboratory and radiologic findings of COVID-19, are milder in neonates than in the older ages. Hence, it can be argued that the prognosis of COVID-19 in the neonatal period is generally good.

    Keywords: Outcome, Clinical Presentation, COVID-19, Neonatal SARS-Cov-2 Infection}
  • Mohamad Hosein Lookzadeh *, Sedigheh Ekraminasab, Fatemeh Baghalsafa
    Background

    Although COVID-19 in pregnant women and their neonates has been verified, its impact on neonates born to infected mothers has remained unclear and there is not enough evidence about how this vertical transmission occurs.

    Case Report

    In this case report, we explained that a neonate girl was born to a mother with COVID-19 infection. Our main goal was to focus on the follow-up and outcome of the neonate. The neonate was at GA = 28 weeks who was born by cesarean section due to respiratory distress of her mother. Also on day 18, she experienced recurrent unilateral seizures so the sample of her cerebrospinal fluid (CSF) was examined.

    Results

    The neonate had a positive reverse transcription polymerase chain reaction (RT-PCR) test for COVID-19, while this neonate after birth, due to mother’s positive PCR, immediately was isolated from the operating room. The neonate’s nasal sample was positive for more than 18 days. Twenty-six days after birth, the neonate was re-evaluated for clinical laboratories, all of which were normal and she had favorable outcomes.

    Conclusion

    In our case report despite the neonate was premature and had seizures, she had favorable outcomes because we quickly started treatment and supportive measures. It is recommended; Symptomatic neonates born to infected mothers must be evaluated for COVID-19 to start proper treatment and quarantine. Additional studies are needed to evaluate the outcomes of COVID-19 in neonates and how to minimize the risk of this disease in neonates.

    Keywords: Neonatal SARS-Cov-2 Infection, COVID-19, Clinical Presentation, Outcome, Vertical transmission}
  • Bayad Mahmood*, Ibrahim Saeed Gataa, Umed Mustafa
    Background and Aim

    Oral cancer is a major public health issue worldwide; it remains a highly lethal and disfiguring disease, it is primarily a disease of epithelial origin, it has various clinicopathological pictures. is to demonstrate various clinical and pathological presentations of oral squamous cell carcinoma in Iraqi population.

    Materials and Methods

    A total of 80 cases of histologically diagnosed squamous cell carcinoma collected from the main centers of Sulaymaniyah teaching hospital/Hiwa cancer center Hospital/Sulaymaniyah/Iraq were analyzed according to age, sex, site, clinical, and pathological presentation of oral squamous cell carcinoma at the time of presentation, and histological grading.

    Results

    Patients in their sixth decade of life were the most commonly affected with a male-tofemale ratio of 1.4:1. The tongue was the most frequently affected site, followed by the floor of the mouth. The most common clinical presentation is ulceration and swelling. More than 40% of the cases were well-differentiated squamous cell carcinoma.

    Conclusion

    Oral cancer is increasingly seen as a major health problem, in line with the general trend in the region, the need for inter-professional health care delivery approaches for reducing oral cancer mortality and improving patients’ quality of life.

    Keywords: Squamous cell carcinoma, Oral cancer, Clinical presentation, Histopathology, Tumor grading}
  • انیس الوله نانکلی، صبا ذاکری، داریوش پورمند، کریم زمان فر*
    زمینه و هدف

    حاملگی مولر به عنوان یکی از بیماریهای حاملگی  بیماری ترفوبلاستیک بارداری (GTD) است که از جفت پدیدار می شود و عنوان یکی از گروه های بیماری طبقه بندی می شود. مول های هیداتی فرم، 1 در هر 1500 تا 2000 بارداری در ایالات متحده تشخیص داده می شوند. به نظر می رسد تغییرات زیادی در توسعه مول وجود دارد و فراوانی آن در شرق آسیا از کشورهای غربی بیشتر است. مول به دو نوع کامل و ناقص تقسیم می شود. هدف ما مقایسه کلینیکی حاملگی کامل مولر و بارداری ناقص مولر در بیمارستان آموزشی امام رضا (ع) در سال های 1385-1397 است.

    روش کار

    در طی یک دوره ده ساله 289 بیمار که از نظر بالینی بارداری مولار داشتند به بیمارستان آموزشی امام رضا (ع) کرمانشاه مراجعه کرده بودند. نتایج این مطالعه بر اساس سونوگرافی، معاینه جسمی، گزارش پاتولوژی و آزمایش انجام شده از بیمار است. تجزیه و تحلیل با استفاده از نرم افزار SPSS نسخه 16 انجام شد. آزمونT ، مجذور کای، آزمون ویلکاکسون.  ارزش P کمتر از 05/0 از سطح معنی دار آماری معنی دار در نظر گرفته شد.

    یافته ها

    در این مطالعه، بیشتر مادران باردار مولر در گروه سنی 25-45 سال قرار داشتند، زیرا در این سن قدرت باروری زیاد است و پس از آن محدوده سنی 15-24 در رتبه دوم قرار دارد. از طرف دیگر، مول جزیی با بالاترین فراوانی در سن 15-24 سال بود. در مطالعه حاضر، 114 زن باردار (1/48 درصد)Nullipar  بودند و 123 نفر (9/51 درصد)  Multipar بودند. اندازه رحم در حاملگی کامل مول بزرگ تر از مول جزیی بود. در این مطالعه فقط اندازه رحم از نظر آماری ارتباط معنی داری با حاملگی مولر داشت (017/0P = ) و بین سایر متغیرها در مطالعه ما و بارداری مولر رابطه معنی داری مشاهده نشد.

    نتیجه گیری

    با توجه به ارتباط معنی دار اندازه رحم و اهمیت آن، باید در مطالعات بعدی به عنوان یک شاخص مهم مورد توجه قرار گیرد.

    کلید واژگان: حاملگی مولر, ارائه بالینی, مولر کامل. بیماری حاملگی Trophoblastic}
    Anisodowleh Nankali, Saba Zakeri, Daryoush Pourmand, Karim Zamanfar*
    Background & Aims

    Molar pregnancy is one of the gestational diseases of pregnancy trophoblastic disease (GTD) which is a free phenomenon and is classified as one of the disease groups. Gestational trophoblastic disease (GTD) is a term that includes a group of tumors that are characterized by abnormal proliferation of human placental gonadotropin trophoblast (hCG); Guide to Encouraging GTD, Administration, and Related Care It is essential to measure these peptide hormones in serum. Hydatid mole is diagnosed in 1 in 1,500 to 2,000 pregnancies in the United States. There seems to be a lot of change in mole development, and it is more prevalent in East Asia than in Western countries. Mole is divided into two types, complete and incomplete. A complete hydatidiform mole has abnormal chorionic villi that can be seen with the naked eye as a mass with clear vesicles. The size of the vesicles varies and often hangs in clusters of thin bases. Conversely, in incomplete mole pregnancies, hydatidiform changes are focal and less severe; Incomplete moles also contain some embryonic tissues. Although both types of moles fill the uterine cavity, their occurrence in the form of tubular pregnancy or other forms of ectopic pregnancy is rare. Over the past few decades, the clinical manifestations of mole pregnancies have changed significantly due to the earlier application of women for prenatal care as well as the widespread prevalence of ultrasound. As a result, most mole pregnancies are diagnosed more than they are enlarged and cause complications. Due to rapid diagnosis, timely evacuation, and careful post-evacuation monitoring for GTN, maternal mortality rate due to molar pregnancy has become rare. The purpose of preoperative evaluations is to identify known known complications such as preeclampsia, hyperthyroidism, anemia, decreased electrolytes due to severe vomiting, and metastatic disease. After molar pregnancy, monitoring is very important to identify subsequent neoplasms. Therefore, moles should be histologically differentiated from other cases of pregnancy failure that cause hydropic analysis of the placenta; These can mimic the hair changes that occur in a mole pregnancy. Classic molar changes may not be seen before the tenth week of pregnancy; Because the villi have not yet grown and the molar stroma may not have been edematous and without blood vessels, other techniques are used to differentiate. One technique uses a difference in ploidy to differentiate between defective (triploid) moles and diploid products. Excluding rare cases, molar pregnancies can be considered the result of chromosomally abnormal fertilizations. The chromosomal composition in a complete mole is generally diploid. Chromosome composition is usually XX46, and both chromosomes are of paternal origin, a phenomenon called androgenesis. Complete moles and non-molar pregnancies with placental hydropic analysis are both diploid. The aim of clinical comparison is complete molar pregnancy and incomplete molar pregnancy in Imam Reza (AS) Teaching Hospital in Kermanshah.

    Methods

    During a twelve-year period, 237 patients who were clinically pregnant were referred to Imam Reza (AS) Teaching Hospital in Kermanshah in 2018-2006. Although sonography is the main method of diagnosing trophoblastic disease, all cases They are not approved at first. The term "snowstorm" is commonly used to describe this view. Ultrasound image of a complete mole contains an echogenic uterine mass that has a large number of echo-free cystic spaces, but no embryo or amniotic sac is seen. It is an embryo or at least an embryonic tissue. However, in early pregnancy, ultrasound will show the above clear appearance in only half of the cases of hydatidiform mole. The results of this study are based on ultrasound, physical examination, pathology report and examination of the patient. Analysis was performed using SPSS software version 16, T test, Chi-square, Wilcoxon test.

    Results

    In this study, the strongest risk factors are age and history of hydatidiform mole in previous pregnancies. Women on both sides of the reproductive age range are at greater risk. Most of molar's pregnant mothers were in the age group of 25-45 years, because at this age the fertility is high, followed by the age range of 24-24. On the other hand, partial moles had the highest frequency at the age of 15-24 years. In the present study, 114 pregnant women (48.1%) were nulliparous and 123 (51.9%) were multiparous. The size of the uterus in full pregnancy was larger than the partial mole (flesh mass). The most common clinical sign was vaginal bleeding. Uterine size in full molar pregnancy was larger than incomplete molar, which was statistically significant. Hyperemesis was higher in complete mole than incomplete mole, although this difference was not significant, but its P. Value level was close to significant and was calculated to be around 0.06. The frequency of complete moles was higher than incomplete moles. The highest frequency of blood group was related to O positive and the lowest frequency of blood group was related to AB negative. Most cases of complete molar pregnancy were 11-17 weeks in gestational age and less than 10 weeks in incomplete moles. Most pregnant mothers had multiple molar pregnancies. The majority of patients with the diagnosis of molar pregnancy were urban. In this study, only the size of the uterus was statistically significantly associated with molar pregnancy (P = 0.017) and no significant relationship was observed between other variables in our study and molar pregnancy.

    Conclusion

    The clinical manifestations of complete molar pregnancy were similar to incomplete molar and were not statistically significant. And in two study groups where complete and incomplete moles were compared. The results showed that the majority of women who had molar pregnancies lived in the city and there was no statistically significant difference. Considering the significant relationship between uterine size and its importance, it should be considered as an important indicator in future studies and is an important and helpful indicator in diagnosing complete mole pregnancy from incomplete mole.

    Keywords: Molar pregnancy, Clinical presentation, Complete mole, Trophoblastic gestational disease}
  • دانیال قاسمی، احمد زارعی، محمدحسین عظیم زاده اردبیلی، عرفان اشجعی، محمدجواد بهزادنیا*
    زمینه و هدف

     در دسامبر 2019، پنومونی ویروسی مرتبط با کرونا ویروس 2019 در ووهان، چین ظاهر شد و پاندمی کووید-19 را ایجاد کرد. به دنبال این پاندمی عوارض و تظاهرات بالینی مختلفی به وجود آمده است و شاهد افزایش مرگ و میر بیماران بسیاری نیز بوده ایم. در این مطالعه به بیان خصوصیات اپیدمیولوژیک، بالینی و تصویربرداری فوت شدگان ناشی از کووید-19 پرداخته ایم.

    روش ها

    در این مطالعه مقطعی در بیمارستان بقیه الله (عج) از ابتدای اسفند ماه 1398 تا پایان اردیبهشت ماه 1399، 3220 بیمار با تظاهرات بالینی مشکوک به کووید-19 پذیرش شدند که 278 مورد منطبق بر معیارهای ورود مطالعه (مرگ ناشی از کووید-19) بودند. اطلاعات دموگرافیک، یافته های بالینی و پاراکلینیکی این بیماران بر اساس مستندات موجود ثبت گردید. در ادامه داده ها در نرم افزار SPSS Ver.26 وارد و سپس مورد تجزیه و تحلیل آماری قرار گرفت.

    یافته ها

    در بازه زمانی یاد شده، 278 بیمار (8/63%) مبتلا به کوید 19 فوت شده در این مرکز وارد مطالعه شدند. از میان افراد فوت شده کووید-19 در این مرکز 207 نفر (74/5%) مرد و 71 نفر (25/5%) زن بودند. میانگین سنی افراد مورد مطالعه 66/01 سال با انحراف معیار 13/71 بود. 193 افراد (69/4%) دارای بیماری زمینه ای بودند. تب (69/8%)، سرفه (53/2%) و تنگی نفس (82/7%) به ترتیب شایع ترین تظاهرات بالینی این افراد بود. نمای Ground Glass Opacity 243 بیمار (87/4%) شایع ترین یافته سی تی اسکن ریه این بیماران بود؛ هرچند در این مطالعه بین الگوی درگیری ریه در سی تی اسکن و میزان اکسیژناسیون خون بدو ورود افراد متوفی ارتباط معنی مشاهده نگردید. همچنین میزان مرگ و میر کووید-19 در این مطالعه 8/63% می باشد.

    نتیجه گیری

    این مطالعه نشان داد که حدود دوسوم فوت شدگان را مردان مسن و حداقل دارای یک بیماری زمینه ای داده اند که توجه ویژه ای را در چگونگی درمان و پیگیری آن ها می طلبد؛ چرا که افزایش زمان بستری در این گروه و بالتبع بار مالی آن بر سیستم سلامت تحمیل می گردد.

    کلید واژگان: کرونا ویروس, کووید-19, مرگ و میر, علائم بالینی}
    Danial Ghasemi, Ahmad Zarei, Mohamadhosein Azimzade Ardabili, Erfan Ashjaei, Mohamadjavad Behzadnia*
    Background and Aim

    In December 2019, a kind of viral pneumonia associated with the 2019 novel coronavirus (2019-nCoV) appeared in Wuhan, China and then a pandemic of COVID-19 created. We aimed to clarify the epidemiological, clinical findings and imaging characteristics of COVID-19 pneumonia.

    Methods

    In this cross-sectional study, after reviewing the records cases of the patients who died from covid-19 referred to the Baqiyatallah hospital, as a referral center in Tehran (20 Feb 2019 to 20 May 2020). In this time, 3220 patients met clinical manifestation of COVID-19 which 278 cases were included in our study. Demographic data and clinical and imaging findings of patients were recorded. The data were entered into SPSS Ver.26 software and analyzed subsequently.

    Results

    278 patients who died from COVID-19 enrolled in the study. The average age was 66.01 (SD 13.7), including 207 (74.5%) men and 71 (25.5%) women. 193 (69.4%) patients at least had an underlying disease. The most common clinical presentations include fever in 194 (69.8%), cough in 148 (53.2%) and shortness of breath in 230 (82.7%) patients. Ground-glass opacity in 243 (87.4%) of the patients was the most apparent finding in their lung CT Scan. The Mortality rate of COVID-19 in this study was 8.63%. although, there was no relationship between the pattern of CT-scan and oxygen saturation in the mentioned patients (P >0.05).

    Conclusion

    This study showed that two-thirds of the death cases were the old men who had a least an underlying disease; this requires a specific consideration on their management and follow-up; wherefore, their more prolonged admission days have a financial load on the health system.

    Keywords: Coronavirus, COVID-19, Mortality, Clinical presentation}
  • Bahram Dehghan, Ahmad Abeshtan Abdullah Sarami, Saied Saeidimehr, Elham Maraghi, Fakher Rahim *
    Objectives

     The aim of the present study was to assess clinical characteristics, management, and in-hospital outcomes of COVID-19 among oil refinery workers in a single referral center.

    Methods

     This cross-sectional study was conducted in a non-COVID single referral center from March to August 2020. At the Naft Grand Hospital, a COVID-19 specimen collection and molecular detection unit was established, and staff were trained how to collect suitable samples (sufficiently deep swabs), store, pack, and transport them. The diagnosis of COVID-19 infection (SARS-CoV-2) was confirmed by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Results

     Overall, 500 patients with confirmed COVID-19 infection were included, among whom the most common comorbidities were hypertension (52.2%) and diabetes (45.6%). Moreover, 298 patients (59.6%) had one to three comorbidities; 148 patients (29.6%) had four to six comorbidities, and two patients (0.4%) suffered from seven and more comorbidities. Out of these, 23 patients (4.6%) had cancer, and 206 (41.2%) suffered from other diseases. Most of the patients (390, 78.8%) received Kaletra, and 387 (78.02%) were treated with Azithromycin. Overall, PCR results were positive in 377 (75.4%) patients; computed tomography scan (CT-scan) was positive in 413 (82.6%), and CRP test rendered positive results in 335 patients (67%).

    Conclusions

     Most referred cases were survivors with mild to moderate symptoms, and a few of them were unfortunately non-survivors. This could be due to the appropriate responses to treatment and institutional isolation of people with mild COVID-19 symptoms. Thus, good and evidence-based clinical care combined with intense public health interventions will save the lives of thousands, if not millions, worldwide.

    Keywords: Clinical Presentation, In-Hospital Outcome, COVID-19 Disease}
  • Nilesh Patel, Kairavi Desai*, Jatin Sarvaiya, Saqlain Malek

     Dengue fever is caused by any one of four types of dengue viruses (DEN1-DEN4), spread mainly by Aedes aegypti. India had the largest number of dengue cases, with about 33 million apparent and another 100 million asymptomatic infections occurring annually. The patients typically present with the sudden onset of fever, frontal headache, retroorbital pain. The laboratory diagnosis can be made by IgM ELISA or by NS1 antigen-detection ELISA during the acute phase. This research was conducted from January 2018 to December 2018 at Sir T. hospital and Government Medical College in Bhavnagar, Gujarat. The patients having complaints of fever, headache, myalgia, arthralgia or rash, were clinically examined, and laboratory investigated for dengue with NS1 and/or IgM dengue antibody. A total of 536 patients was screened, of which 112 patients were diagnosed as dengue fever at 21% dengue positivity rate, based on detection of NS1 (46/304, 15%), and anti-dengue IgM (66/232, 28%) in their sera. The majority of the patients were males (77/112, 69%). The majority of patients were in 11–30 years’ age group (66/316, 21%). Fever (100%) was the chief presenting complaint, followed by headache (83, 93%), and myalgia (79, 89%). The highest number (28) of dengue patients was observed in the month of October 2018. According to this study results, the physicians in the dengue-endemic area should be aware of dengue in acute febrile illnesses and use the appropriate laboratory tests such as NS1 antigen and IgM antibodies for early dengue diagnosis. This can help clinicians to prevent morbidity and mortality associated with dengue.

    Keywords: Clinical presentation, Dengue, Laboratory tests}
  • Zahra Davoudi, Arezoo Chouhdari, Hooman Bahrami, Motlagh *, Karim Bagheri
    Background
    Thyroid nodules are frequent occurrences. This study aims to evaluate the risk of malignancy based on the 2015 American Thyroid Association Management: Guidelines for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer.
    Methods
    In this cross-sectional study, ultrasonography and clinical manifestations were compared with pathology findings to predict the risk of malignancy in thyroid nodules. Assessment of the ultrasound findings was based on the criteria recommended by The 2015 American Thyroid Association Management Guidelines for Thyroid Nodules. For the evaluation of the association between clinical and ultrasound findings with histopathology results, we used the chi-square and Fisher’s exact tests. The relative risk and prediction of malignancy was assessed by multiple logistic regression analysis. Data analysis was performed by the SPSS19. The significance level was set at P<0.05.
    Results
    From 130 patients with thyroid nodules, 110 (84.6%) were female. The mean age of participants was 46.1±11.5 years. Histopathology findings showed malignancy in 17.7% of the nodules, all of were papillary thyroid carcinoma. Multivariate logistic regression showed some of the ultrasonography parameters, absence of halo (P<0.001, OR=28), taller than wide shape (P=0.001, OR=18.3), nodule size more than 4 cm (P=0.04, OR=12.1), irregular margin (P=0.001, OR=10.06), solid or mixed composition (P=0.002, OR=8.1), hypoechoic (P=0.001, OR=4.5), lymph node positive  (P=0.002, OR=4.3), positive calcification (P=0.03, OR=2.08), positive internal vascularity (P<0.001, OR=1.05), and intermediate/high level of suspicion (P=0.001, OR=12) could predict malignancy in patients with thyroid nodules.
    Conclusion
    Based on increasing rate of thyroid cancer, in this study, the new and accurate ultrasound technique is recommended as alternative diagnostic method due non-invasive nature and lower cost used.
    Keywords: Thyroid nodules, Clinical presentation, Ultrasonography, Malignancy, Pathology}
  • Rajendra Prasad Takhar*, Kiran Mirdha, Gopal Purohit, Lokesh Maan, Mahendra Kumar Bainara
    Background
    The Human Immunodeficiency Virus (HIV) has long been known to alter the clinical presentation of tuberculosis (TB), which varies according to the time of occurrence of TB infection and the level of immunodeficiency. Identifying variations in clinical features in HIV-TB coinfection might be helpful in settings with limited diagnostic facilities. The aim of this study was to assess the clinical presentation of TB in HIV coinfection and associate clinical findings with level of immune suppression (CD4 count).
    Materials and Methods
    In this prospective, cross-sectional observational study 110 patients having TB-HIV co-infection were assessed for clinical presentation and correlation with CD4 count. The study setting was a tertiary care teaching hospital. Patients were categorized in three group based on CD4 counts as group I: ≤ 100 cells/cmm, group II: 101-200 cells/cmm and group III: > 200 cells/cmm.
    Results
    110 patients were enrolled, 70% had CD4 cell count < 200 cells/mm3. Mean age and CD4 cell were 33.82±8.79 years and 181.7cells/cmm, respectively. Most common form of tubercular involvement was pulmonary (56.4%) followed by combined pulmonary and extra-pulmonary involvement (28.2%) and exclusively extra-pulmonary (15.5%). No significant intergroup difference was observed in site of involvement among three groups (p=0.700). Cough (91.8%) followed by low grade fever (85.5%), anorexia (82.7%) and weight loss (66.4%) were the commonest presenting symptom without any significant inter group difference. 70.9% patients were in undernourished category and 53.6% were febrile on examination. Sputum negative TB was noted 53.8%. 72.0% of patients with CD4 counts ≤100 had sputum negative TB as compared to sputum positive TB (28%).
    Conclusion
    Due to varied clinical presentation of TB in HIV patients, ample knowledge of the clinical spectrum at different levels of immunosuppression is absolutely necessary to identify such patients early. Key words: HIV infection, TB, Clinical presentation, Immune-suppression, Acid Fast Bacilli
    Keywords: HIV infection, TB, Clinical presentation, Immune-suppression, Acid Fast Bacilli}
  • Seyedeh Nina Masoom*, Arash Havaei

    Chediak-Higashi syndrome (CHS) is an inherited primary immunodeficiency with an autosomal recessive pattern which is usually identified by partial albinism and frequent pyogenic infections. Herein, we report the interesting case of childhood onset with the main presentation of chronic diarrhea which was treated with dexamethasone and various antibiotics for achronic fever. The patient was givenetoposide once a week and intravenous immunoglobulin monthly thereafter, which caused partial shrinkage in the size of the liver and spleen and improved the patient’s clinical condition. Since CHS is invariably lethal after entering the accelerated phase and early diagnosis may facilitate bone marrow transplantation as the only curative treatment, careful examination in unusual patients without multiple recurrent infections or diagnosed hemophagocytic lymphohistiocytosis should be considered.

    Keywords: Primary immunodeficiency, Clinical presentation, Chediak-Higashi syndrome}
  • Jafar Nasiri, Mohammadreza Ghazzavi *, Omid Yaghini, Mohammadreza Chaldavi
    Background
    Considering the fact that there are no reports about the clinical presentations and outcome of Guillain-Barré syndrome (GBS) in our region, we aimed to report some mentioned findings in children diagnosed with GBS in Isfahan, Iran.
    Materials And Methods
    In this retrospective study, pediatric patients diagnosed with GBS were enrolled.The following information were extracted from the medical files of patients; age, gender, early signs and symptoms of GBS, neurological features, sensory and motor and autonomic involvements, sphincter dysfunction, bulbar muscle involvement, respiratory failure, cranial nerve paralysis, delay time from onset to definite diagnosis and management of GBS and the outcome.
    Results
    During this study, 57 children with GBS aged 1-13 years were evaluated. Frequency of GBS was significantly higher in boys than in girls (38.6% vs. 61.4%, P=0.01, OR=0.39). The most common clinical presentations were distal lower limb weakness (92.11%), reduced deep tendon reflex (DTR ) (82.46%) and neuropathic pain (75.44%). 92.9% of patients had complete recovery.
    Conclusion
    The findings of this study indicated that distal lower limb weakness, reduced deep tendon reflex and neuropathic pain are the main clinical presentation in children with GBS but in some patients DTR may be normal or even exaggerated in early stage of disease. This finding suggests that revising the diagnostic criteria for GBS may be necessary. Most of our patients had complete recovery. The only death was due to autonomic involvement.
    Keywords: Guillain-Barré, children, outcome, clinical presentation}
  • Kamal Rashidiazar, Aliasghar Darzi, Sekineh Kamali Ahangar, Sepideh Siadati, Abdolrahim Gholizadehpasha *
  • Iman Karimzadeh *, Behrooz Heydari, Hossein Khalili, Esfandiar Shojaei, Abdolrasool Ebrahimi
    Background/
    Objective
    The aim of the present preliminary study was to assess the demographic, clinical, paraclinical, microbiological, echocardiographic, and therapeutic profile as well as in-hospital outcome of patients with infective endocarditis at a referral center for various infectious diseases in Iran.
    Methods
    Required demographic, clinical, plausible complications and paraclinical data were collected from patients’ medical charts. Echocardiographic findings were obtained by performing transthoracic and/or transesophageal echocardiography as clinically indicated. In addition, details of management modalities and in-hospital outcome of patients were recorded.
    Results
    During a 3-year period, 55 patients with definite or possible diagnosis of Infective endocarditis were admitted to the ward. Twenty one (38.2%) patients were injection drug users. Staphylococcus aureus and S. epidermidis were the most commonly isolated microorganisms. Management modalities of Infective endocarditis included antimicrobial therapy alone (48 cases) and the combination of antimicrobial therapy and surgery (7 cases).
    Conclusion
    The rate of negative blood culture in our cohort is high. S. aureus and S. epidermidis were the most commonly isolated microorganisms from positive blood cultures. Congestive heart failure was the most frequent infective endocarditis complication as well as indication for surgery. In-hospital mortality rate of patients was unexpectedly low.
    Keywords: Infective endocarditis, clinical presentation, treatment, outcome}
  • حسین سلیمانی صالح آبادی *، سعید صالحی نژاد کوویی، محمد باقر اولیاء، علی دهقان، مسعود محمدی
    زمینه و هدف
    اسپوندیلیت انکیلوزان (Ankylosing Spondylitis، AS) یک بیماری التهابی است که به طور عمده اسکلت محوری بدن را مبتلا می کند، تفاوت های تظاهرات بالینی بیماری اسپوندیلیت انکیلوزان در مردان و زنان، مطرح کننده تاثیر احتمالی جنسیت بر شدت بیماری است. این مطالعه به منظور بررسی تفاوت های تظاهرات بالینی بیماری اسپوندیلیت انکیلوزان انجام شد.
    روش بررسی
    115 بیمار مبتلا به اسپوندیلیت انکیلوزان مراجعه کننده به کلینیک روماتولوژی از فروردین 1380 تا اسفند 1392 در یک مطالعه مقطعی در شهر یزد مورد ارزیابی قرار گرفتند. مهم ترین متغیرهای مورد ارزیابی شامل داده های دموگرافیک، تظاهرات بالینی، مرحله رادیوگرافی درگیری ساکروایلیاک و داده های آزمایشگاهی بود که از پرونده های بیماران استخراج و در پرسش نامه ها ثبت شد.
    یافته ها
    هر دو گروه از نظر سن تشخیص بیماری، وجود انتزیت (التهاب یا درد در محل اتصال تاندون یا رباط به استخوان)، درگیری مفاصل محیطی و داده های آزمایشگاهی مانند سرعت رسوب گلبول های قرمز (ESR)، پروتئین واکنشی C (CRP) و هموگلوبین با یکدیگر همسان بودند. درد التهابی گردن در مردان بیشتر از زنان بود (2/77% در مقابل 8/51% (01/0P=). مطالعات رادیوگرافی ساکروایلیاک نشان داد که 3/11% از مردان و 37% از زنان، در مرحله اول (009/0P=) و 2/27% از مردان و 7/3% از زنان، در مرحله چهارم (001/0P=) قرار دارند که از نظر آماری اختلاف معناداری داشت.
    نتیجه گیری
    مدت زمان بین سن شروع علایم و سن تشخیص بیماری، درد التهابی گردن و مراحل پیشرفته درگیری مفاصل ساکروایلیاک در مردان نسبت به زنان بیشتر دیده شد. با وجود اینکه این یافته ها مطرح کننده این است که جنسیت می تواند بر الگو و شدت بیماری اسپوندیلیت انکیلوزان تاثیر داشته باشد.
    کلید واژگان: اسپوندیلیت آنکیلوزان, تظاهرات بالینی, جنسیت}
    Hossain Soleymani Salehabadi *, Saeid Salehinejad Kouvei, Mohammad Bagher Owlia, Ali Dehghan, Masoud Mohammadi
    Background
    Ankylosing spondylitis (AS) is an inflammatory disease that mainly affects axial skeleton of the body and ankylosing spondylitis ligaments around the spine at the junction of the spine are inflamed, because the disease is progressive and can lead to significantly cause of disability and the studies could provide a mechanism for the early detection of the disease or help determine when to start treatment, the difference in clinical presentations of AS in men and women is indicative of potential effect of gender on severity of the disease. This study was conducted with the aim to investigate the effect of gender on severity of AS.
    Methods
    In a cross-sectional study, one hundred and fifteen patients with ankylosing spondylitis who referred to Yazd Rheumatology Clinic between 2001 and 2013 were evaluated. Sampling was performed using non-random convenient method. The most important variables studied included demographic data, clinical presentation, radiographic stage of sacroiliac involvement, and laboratory data extracted from patients’ files and recorded in questionnaires.
    Results
    Both groups according to age at diagnosis, presence of enteritis, peripheral joint involvement and laboratory data such as C-reactive protein (CRP), erythrocyte sedimentation rate (ESR) and hemoglobin were matched. Inflammatory neck pain was more prevalent in men than in women (77.2% against 51.8%; P
    Conclusion
    According to the results of the study, the time between age of onset and age at diagnosis, inflammatory pain in the neck and advanced stage in men than in women was higher. Although these findings suggest that gender may have an impact on the pattern and severity of AS but the time delay in diagnosis as a disease affecting the intensity and pattern should not be overlooked.
    Keywords: ankylosing spondylitis, clinical presentation, cross, sectional studies, gender}
  • Majid Akrami, Ali Ghaeini Hesarooeih, Maryam Barfei, Vahid Zangouri, Zahra Alborzi
    Objective
    To determine the epidemiological, clinical, laboratory characteristics as well as outcome of 411 patients with bowel obstruction in Southern Iran.
    Methods
    This was a cross-sectional study being performed in Shahid Faghihi hospital of Shiraz between 2006 and 2012. We reviewed the medical charts of the 411 patients with initial diagnosis of bowel obstruction who were admitted to our center during the study period. The patients’ demographic, clinical and laboratory findings as well as their management and outcome was recorded in data gathering forms. The data were then analyzed according to the outcome and clinical characteristics.
    Results
    Among the 411 patients with initial diagnosis of bowel obstruction, 253 (61.5%) were men and 158 (38.5%) were women. The mean age of the patients was 48.2±19.7 years. Besides, 73.6% were observed and 26.4% were operated. Those who were operated had those who underwent operation had significantly lower frequency of obstipation (28.1% vs. 71.9%; p=0.045) and abdominal distention (32.3% vs. 67.7%; p=0.007). Intraoperative findings included adhesion band formation in 50 (48.1%), mass 18 (17.3%), and hernia 7 (6.7%). We found that the frequency of malignancy was significantly higher in those who were managed conservatively compared to those undergoing operation (64.3% vs. 35.7%; p=0.042). The mean hospital stay was significantly higher in those who underwent operation (8.1 ±7.5 vs. 2.6±2.2 days; p=0.035).
    Conclusion
    The results of this study demonstrates although some signs and symptoms, such as abdominal pain, vomiting, abdominal tenderness, abdominal distention, and obstipation, were more common among the patients with bowel obstruction, they were not sensitive and specific enough for definite diagnosis. Due to the lack of positive predictive value of clinical signs and symptoms in diagnosis of bowel obstruction, a reasonable and logical modality is needed for bowel obstruction diagnosis with better accuracy.
    Keywords: Bowel obstruction, Clinical presentation, Characteristics, Laparatomy, Malignancy}
  • شهریار امیرحسنی، ساسان محرابی*، عبدالمجید ایلون کشکولی
    زمینه و هدف

    اپیدیدیموارکیت بیماری نسبتا شایعی است که علاوه بر نایسریا گنوره، کلامیدیا و اشیریشیا کلی، تب مالت (بروسلوز) هم یکی از علل مهم این بیماری به خصوص در مناطق اندمیک به شمار می رود. هدف این مطالعه ارزیابی جنبه های اپیدمیولوژیک و یافته های بالینی اپیدیدیموارکیت بروسلایی و مقایسه آن با نوع غیر بروسلایی در استان همدان است.

    مواد و روش کار

    در این مطالعه مقطعی 115 بیمار مبتلا به اپیدیدیموارکیت که بصورت سرپایی یا بستری درمان شده اند، در دو گروه بروسلایی با 38 بیمار و غیر بروسلایی با 77 بیمار در مدت شش سال مورد ارزیابی قرار گرفته و نتایج با هم مقایسه شده اند.

    یافته ها

    از نظر میانگین سنی، وضعیت تاهل، سمت درگیری، مواجهه شغلی و فصل بروز بیماری بینی گروه ها تفاوت معنی داری وجود نداشت. نوع بروسلایی بیشتر در میان روستاییان و عشایر و نوع غیر بروسلایی بیشتر در شهر نشین ها دیده شد (02/ 0 p =).

    نتیجه گیری

    در مناطق اندمیک از نظر بروسلوز مانند کشور ما، جراحان کلیه و مجاری ادرار باید احتمال ابتلا به نوع بروسلایی را مخصوصا در موارد پیچیده، عود کرده، مقاوم به درمان و یا در افراد دارای مشاغل مرتبط مد نظر قرار داده و بررسی های لازم را برای رد بیماری تب مالت انجام دهند.

    کلید واژگان: تب مالت, بروسلوز, اپیدیدیمیت, ارکیت, اپیدمیولوژی, علایم بالینی}
    Sh Amirhassani, S. Mehrabi *, A. Iloon Kashkouli
    Background And Objectives

    Epididymoorchitis is relatively common disease that in addition to Neisseria gonorrhea, Chlamydia trachomatis and Escherichia coli, Brucella must be considered as an etiologic factor especially in endemic area. The aim of current study is comparison of epidemiologic and clinical presentation of brucella epididymoorchitis with nonbrucella epididymoorchitis in Hamadan Province.

    Materials And Methods

    During this cross sectional study, 115 epididymoorchitis patients that were treated inpatient or outpatient, evaluated as 2 groups either brucella epididymoorchitis (group1= 38) or nonbrucella epididymoorchitis (group 2 = 77) during 6 years.

    Results

    There were not seen statistical differences in mean age, marital status, side of involvement, occupational exposure, and the illness occurrence season between the groups. Brucella epididymoorchitis were seen more in rural living patients and nonbrucella epididymoorchitis in town living cases (p=0.02).

    Conclusion

    In brucellosis endemic areas such as Iran, urologists should be consider the likelihood of brucella epididymoorchitis especially in complex, recurrent, treatment resistant and occupational exposure patients with careful history, physical examination and laboratory evaluation.

    Keywords: Epididymitis, Orchitis, Brucella, Epidemiology, Clinical presentation}
نکته
  • نتایج بر اساس تاریخ انتشار مرتب شده‌اند.
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