scholarly journals Arthroscopic Removal of Suprapatellar Fibroma of Tendon Sheath

2017 ◽  
Vol 03 (02) ◽  
pp. e58-e61 ◽  
Author(s):  
Nan Lou ◽  
Christian Fang ◽  
Frankie Leung ◽  
Florence Cheung ◽  
Tak Wong
Keyword(s):  
Case Report ◽  
Knee Joint ◽  
Rare Disease ◽  
Clinical Presentation ◽  
Tendon Sheath ◽  
Chinese Patient ◽  
Arthroscopic Removal

AbstractIntra-articular fibroma of tendon sheath is a rare disease. To our knowledge, less than 20 cases have been reported in the literature, and none of them was a Chinese patient. In this case report, we present a Chinese patient with intra-articular fibroma of tendon sheath of the knee joint which was excised arthroscopically. We also summarized the clinical presentation, diagnosis, and subsequent management of intra-articular fibroma of tendon sheath.

scholarly journals Juvenile Systemic Sclerosis- A Case Report

2018 ◽  
Vol 29 (2) ◽  
pp. 70-72
Author(s):  
ASMM Rahman ◽  
MB Uddin
Keyword(s):  
Case Report ◽  
Systemic Sclerosis ◽  
Rare Disease ◽  
Clinical Presentation ◽  
Organ Involvement ◽  
Published Data ◽  
Multisystem Disorder ◽  
Adult Disease ◽  
Adult Form ◽  
Juvenile Systemic Sclerosis

Juvenile systemic sclerosis (JSS) is a multisystem disorder as well as rare disease of childhood, and the amount of published data is limited. It appears that its clinical presentation differs from adult disease and the limited form affects only very few children. The organ involvement pattern differs also from the adult form. Prognosis seems to be better with a 5-yr survival of 95% of the JSS patients. Though the incidence is very rare but we describe a 10-yr-old boy who presented with typical features of JSS.TAJ 2016; 29(2): 70-72

scholarly journals Chronic Recurrent Multifocal Osteomyelitis of The Shoulder: A Case Report

1970 ◽  
Vol 14 (2) ◽  
pp. 248-252 ◽  
Author(s):  
Ki Won Lee ◽  
Young Joon Choi ◽  
Hyung Sun Ahn ◽  
Chung Hwan Kim ◽  
Jae Kwang Hwang ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Disease ◽  
Clinical Features ◽  
Clinical Presentation ◽  
Chronic Recurrent Multifocal Osteomyelitis ◽  
Arthroscopic Debridement ◽  
Multifocal Osteomyelitis

PURPOSE: We report a case of chronic recurrent multifocal osteomyelitis of the shoulder.MATERIALS AND METHODS: A 16 year-old male who had suffered from chronic recurrent multifocal osteomyelitis of the shoulder was diagnosed by clinical features and biopsy and was treated with arthroscopic debridement and Naproxen.RESULTS: Symptoms was subsided without relapse during 16 months follow up.CONCLUSION: Chronic recurrent multifocal osteomyelitis is rare disease and it can be misdiagnosis because of its rarity and non-specific clinical presentation. This is a report of a case of chronic recurrent multifocal osteomyelitis of the shoulder in 16 years man.

scholarly journals Grisel Syndrome: Case Report

2017 ◽  
Vol 39 (01) ◽  
pp. 037-040
Author(s):  
Bruno Roncaglio ◽  
Tadeu Gervazoni Debom ◽  
Marcus Alexandre Novo Brazolino ◽  
Thiago Cardoso Maia ◽  
José Lucas Batista Filho ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Disease ◽  
Clinical Presentation ◽  
Present Report ◽  
Upper Airways ◽  
Infectious Process ◽  
Grisel Syndrome

AbstractWe report a case of a rare disease, Grisel syndrome, which manifests as a kind of rotational fixation of the atlas on the axis, resulting from an infectious process of the upper airways. In the present report, we discuss etiology, clinical presentation, diagnosis, treatment and outcome after intervention.

scholarly journals Creutzfeldt-Jakob Disease Presenting with Dementia and Mimic a Stroke During One Year: Case Report and Review of Literatures

2019 ◽  
Vol 8 ◽  
pp. e1357
Author(s):  
Alireza Vakilian ◽  
Mohaddaseh Fekri ◽  
Habib Farahmand
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Disease ◽  
Clinical Manifestation ◽  
Clinical Presentation ◽  
Chief Complaint ◽  
The Other ◽  
Progressive Dementia ◽  
Jakob Disease ◽  
One Year

Background: Creutzfeldt-Jakob disease (CJD) is a progressive and fatal prion disease in human and its annual incidence is estimated one per million. Sporadic form of CJD is the most common form of the disease that involved 85% of cases. Case Report: We presented two cases of CJD with the different clinical presentation; a 58-year-old woman who referred with amnesia, depression and a 59-year-old woman with ataxia as her chief complaint. Based on the findings and roled-out the other differential diagnosis, the CJD was confirmed. Both of them died before 12 months after diagnosis. Conclusion: Although CJD is a rare disease with different clinical manifestation, it is considered as one the differential diagnosis of progressive dementia.[GMJ.2019;8:e1357]  

scholarly journals Pseudomyxomaperitonei: A Rare Clinical Entity - A Case Report

Pulse ◽  
2018 ◽  
Vol 10 (1) ◽  
pp. 47-51
Author(s):  
MF Hossain ◽  
MD Hossain ◽  
M Begum ◽  
AMO Shamsi
Keyword(s):  
Case Report ◽  
Rare Disease ◽  
Clinical Presentation ◽  
Primary Tumour ◽  
Treatment Options ◽  
Abdominal Cavity ◽  
Diagnostic Procedures ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Uncommon Disease

Pseudomyxomaperitonei (PMP) is a rare disease characterized by presence of gelatinous ascites and mucinous implants on the peritoneum and omentum. We report the case of a 58 years old woman with primary tumour of the appendix and secondary involvement of other structures & organs of abdominal cavity. Aim of this case report is to create awareness among the clinicians regarding this uncommon disease presented with ascites and irregular masses in the abdomen. In addition, literature on the clinical presentation, diagnostic procedures, and treatment options has been briefly reviewed.Pulse Vol.10 January-December 2017 p.47-51

Creutzfeldt-Jakob Disease Presenting with Dementia and Mimic a Stroke During One Year: Case Report and Review of Literatures

2019 ◽  
Vol 8 ◽  
pp. 1357
Author(s):  
Alireza Vakilian ◽  
Mohaddaseh Fekri ◽  
Habib Farahmand
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Disease ◽  
Clinical Manifestation ◽  
Clinical Presentation ◽  
Chief Complaint ◽  
The Other ◽  
Progressive Dementia ◽  
Jakob Disease ◽  
One Year

Background:  Creutzfeldt-Jakob disease (CJD) is a progressive and fatal prion disease in human and its annual incidence is estimated one per million. Sporadic form of CJD is the most common form of the disease that involved 85% of cases. Case Report: We presented two cases of CJD with the different clinical presentation; a 58-year-old woman who referred with amnesia, depression and a 59-year-old woman with ataxia as her chief complaint. Based on the findings and rolled-out the other differential diagnosis, the CJD was confirmed. Both of them died before 12 months after diagnosis. Conclusion: Although CJD is a rare disease with different clinical manifestation, it is considered as one the differential diagnosis of progressive dementia.[GMJ.2019;inpress;e1357]

scholarly journals Post-traumatic tenosynovial chondromatosis following a triquetrum fracture: a case report

2021 ◽  
Vol 2021 (4) ◽  
Author(s):  
Danny Mangual ◽  
Gerardo Olivella ◽  
Norman Ramirez ◽  
Eric Astacio ◽  
Juan Bibiloni ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Benign Tumor ◽  
Clinical Presentation ◽  
Ventral Side ◽  
Tendon Sheath ◽  
Common Reason ◽  
Synovial Lining ◽  
Post Traumatic ◽  
Tenosynovial Chondromatosis

ABSTRACT Tenosynovial chondromatosis (TC) is a rare progressive benign tumor from the synovial lining of tendon sheath. The TC mostly affects males between the ages 30 to 50 years old at the ventral side of wrist. There are two different forms of TC that have been proposed in previous studies: an idiopathic cause (primary TC) and a joint related diseases cause (secondary TC). Even though trauma has been written to be a common reason for TC, a case of a secondary TC affecting the dorsal wrist following a triquetrum fracture has never been written before. The aim of this report is to present a rare case of a solitary post-traumatic TC at the dorsal wrist following a triquetrum fracture. We describe the clinical presentation, imaging modalities, histopathological and treatment challenges to manage this difficult lesion.

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