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:: Search published articles ::
Showing 45 results for Type of Study: case report

Somaieh Matin, Yousef Imani Marani, Hossein Salehzadeh,
Volume 19, Issue 3 (10-2019)
Abstract

 
Background: Primary sclerosing cholangitis is a rare and progressive cholestatic disease characterized by narrowing of the biliary tract. Despite high levels of ulcerative colitis, early diagnosis of primary sclerosing cholangitis before the diagnosis of inflammatory bowel disease is rarely reported.
Case history: A 28-year-old woman with no history of medical disease visited our clinic because of a mild generalized pruritus. In initial blood laboratory tests with elevated liver enzymes was observed. In Magnetic resonance cholangiopancreatography (MRCP) was introduced primary sclerosing cholangitis to the patient. Therefore, the patient was under colonoscopy and extensive colitis with terminal ileum involvement was detected and the diagnosis of ulcerative colitis was confirmed in the pathology.
Conclusion: Patients diagnosed with primary sclerosing cholangitis should undergo biopsy colonoscopy to rule out inflammatory bowel disease, even if they have no digestive tract symptoms
Ali Hossain Samadi, Zahra Azimi, Atabak Alafasgari,
Volume 21, Issue 1 (4-2021)
Abstract

Pulmonary alveolar microlithiasis is a rare autosomal recessive disease characterized by the formation of calcium phosphate deposition in the alveoli. Although the disease most often occurs in children, most patients with the disease are diagnosed in adulthood due to the slow progression of the disease inside the lungs. In childhood, it often causes no symptoms, and changes in the lung parenchyma are usually detected by chance. Symptoms usually appear in the third or fourth decade of life. Diagnosis is made with a combination of positive chest radiography and tissue examination. Genetic testing makes it possible to identify other unidentified patients in the patient's family. In the present study, a patient with pulmonary alveolar microlithiasis was diagnosed using imaging and other disease findings, including clinical manifestations as well as history is taken from the patient.
 
Shafagh Aliasgarzade, Mohammad Negaresh, Vahideh Aghamohammadi, Nazli Javaheri, Javad Aliasgarzade, Sevda Mikaeili Mirak,
Volume 21, Issue 4 (1-2022)
Abstract


Neuroarthropathy occurs following the loss of pain sensation in a joint. Martin Charcot was the first researcher who explained this strange, non-infectious destruction of bone and joints. This disease mostly affects the lower extremity of patients, especially their feet and ankle. In this paper, we present a rare case of simultaneous neuroarthropathy in the wrist and ankle of a 39-year-old man with no history of diabetes. Simultaneous neuroarthropathy of two joints and its occurrence in uncommon parts of the body like the wrist is quite rare and might lead to misdiagnosis and incorrect treatment.
 
Soheila Derisavy Jorfian, Emran Hajmohammadi, Erfan Belalzadeh,
Volume 21, Issue 4 (1-2022)
Abstract

Intraosseous mucoepidermoid carcinoma is a rare lesion that is mostly seen in the mandible and in the premolar and molar region. In some cases, clear cells can be seen, which makes it difficult to diagnose.
The purpose of this case report is the clinical and histopathological evaluation of the clear cell variant of hntraosseous mucoepidermoid carcinoma in the anterior region of the lower jaw that was referred to the dentistry faculty of Ardabil University of Medical Sciences.


 
Effat Iranijam, Mohammad Hossein Hosseini, Mohammad Negaresh, Elham Yousefi Ardabili,
Volume 22, Issue 4 (1-2023)
Abstract

A severe acute respiratory syndrome caused by coronavirus 2 infection (COVID-19)was identified in December 2019 and caused a massive pandemic that claimed millions of lives worldwide. The Chimpanzee adenovirus vector vaccine is one of the few vaccines against coronavirus disease in 2020. This case report introduces, a patient who developed thrombocytopenia, fever, and lethargy nine days after vaccination with the chimpanzee adenovirus carrier vaccine. The patient was admitted to the hospital and thrombotic thrombocytopenic purpura (TTP) symptoms appeared during hospitalization.

 

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مجله دانشگاه علوم پزشکی اردبیل Journal of Ardabil University of Medical Sciences
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