A rare case of tumid lupus erythematosis in a patient with fabrys disease – case report

Pathology ◽  
2021 ◽  
Vol 53 ◽  
pp. S36
Author(s):  
Corey Stone ◽  
Peter Peters ◽  
Timothy Willis
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Disease Case ◽  
Fabrys Disease

scholarly journals Lengthy Diagnostic Challenge in a Rare Case of Pulmonary Veno-Occlusive Disease: Case Report and Review of the Literature

2011 ◽  
Vol 50 (12) ◽  
pp. 1323-1327 ◽  
Author(s):  
Xiao-qun Ye ◽  
Chun-song Yan ◽  
Xin-yi Zhang ◽  
Yin Cai ◽  
Feng Guo ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Occlusive Disease ◽  
Review Of The Literature ◽  
Diagnostic Challenge ◽  
Disease Case

scholarly journals Hirayama Disease: Case report of a rare case in Brazil

2021 ◽  
Author(s):  
Larissa Damian Resende ◽  
Thiago de Abreu Silva Pinto ◽  
Henrique Marreiros Veloso Carneiro ◽  
Fellype Matos do Prado
Keyword(s):  
Case Report ◽  
Upper Limb ◽  
Spinal Canal ◽  
Rare Case ◽  
Clinical History ◽  
Resonance Imaging ◽  
Hirayama Disease ◽  
Dural Sac ◽  
Disease Case ◽  
The Right

Context: Hiravama’s disease (HD) is a rare neurological condition described by keizo Hirayama in 1959, in which growth of the content of the spinal canal displaces the posterior dural sac previously when flexing the neck at the level of C7 and T1. Thus, it generates ischemic damage in the cells of the anterior spine. In this context, we present a case report about the disease. Case report: Male, 13 years old, complaining of difficulty in grasping his right hand for 5 months and atrophy in his right upper limb for 1 month. On physical examination, the neurological changes found were: Decreased strength of the right upper limb distally, the deep hypoactive reflexes in both upper limbs. Magnetic resonance imaging of the flexed cervical spine showed stenosis of the C5 to T1 spinal canal, flow-voids prominence in the posterior epidural space (suggestive of venous engorgement), tapering and alteration of T2 signal in the C5-C6 medulla. These findings and along with the clinical history confirmed the diagnosis of HD. Conclusion: HD is a rare disease that needs to be known. Thus, the present study expands the database about the disease, which if diagnosed early, improves the patient’s prognosis.

Large Vulvar Lipoma in an Adolescent: A Case Report

JMS SKIMS ◽  
2011 ◽  
Vol 14 (1) ◽  
pp. 28-29
Author(s):  
R K Maurya ◽  
Pawan Kumar Singh ◽  
Sandeep Singh
Keyword(s):  
Case Report ◽  
Epithelial Cell ◽  
Adolescent Girl ◽  
Rare Case ◽  
Mesenchymal Cell ◽  
Benign Tumors ◽  
Melanocytic Tumors

Lipomas of vulva have been reported only rarely. Benign tumors of the vulva are normally classified according to their origin as epithelial cell tumors (e.g., keratinocytic, adnexal and ectopic tumors), or mesenchymal cell tumors (e.g., vascular, fibrous, muscular, neural, adipose and melanocytic tumors). Vulvar lipomas need to be differentiated from liposarcomas, which are rare but are very similar to lipomas clinically. Here we present a rare case of large vulvar lipoma in an adolescent girl. JMS 2011;14(1):28-29

Primary neuroendocrine carcinoma of renal: a rare case report

2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko
Keyword(s):  
Case Report ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Rare Case Report

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

2017 ◽  
Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Rare Case ◽  
Adrenal Hyperplasia ◽  
Rare Case Report

Empyema due to salmonella typhi in a diabetic patient: a rare case report

2011 ◽  
Vol 3 (6) ◽  
pp. 405-406
Author(s):  
Dr. Nale Swati S Dr. Nale Swati S ◽  
◽  
Dr.Ghadage Dnyaneshwari P ◽  
Bhore Arvind V
Keyword(s):  
Case Report ◽  
Diabetic Patient ◽  
Rare Case ◽  
Salmonella Typhi ◽  
Rare Case Report
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