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Chantelli Razafindrazoto
Chantelli Razafindrazoto

Public Documents 5
Pseudomyxoma peritonei induced by a well-differentiated appendicular mucinous adenoca...
Nitah Randramifidy
Mirana Ranaivoson

Nitah Randramifidy

and 14 more

June 06, 2022
Pseudomyxoma peritonei (PMP) remains difficult to diagnose and has a guarded prognosis. Pseudomyxoma peritonei is a rare entity, of appendicular origin in the majority of cases. Its clinical symptomatology is not specific, the diagnosis is evoked by imaging and surgery, and confirmed by histology.
Arteria Lusoria: A rare cause of chronic dysphagia
Hasina Laingonirina
Andry Rakotozafindrabe

Domoina Hasina Laingonirina

and 7 more

July 09, 2021
Arteria lusoria is a rare vascular malformation. It remains a rare cause of dysphagia which should be considered in the face of any dysphagia unexplained by the usual endoscopic and radiological investigations.
Inappropriate prescription of corticosteroid therapy during inflammatory ileo-colitis...
Chantelli Razafindrazoto
Nitah Randramifidy

Chantelli Razafindrazoto

and 11 more

March 05, 2021
The similarity between intestinal tuberculosis and Crohn's disease could lead us to erroneously prescribe corticosteroid therapy. Therefore, it is essential to differentiate the two pathologies because of the therapeutic implications of Crohn's disease, which can lead to an explosion of tuberculosis symptoms.
Difficulties in diagnosing and managing autoimmune hepatitis in low-income countries
Chantelli Razafindrazoto
Andry Rakotozafindrabe

Chantelli Razafindrazoto

and 9 more

March 05, 2021
The diagnosis of autoimmune hepatitis remains difficult in low-income countries due to the unavailability of the biopsy. autoimmune hepatitis must be retained on the basis of clinical-biological, radiological and immunological criteria. Careful trial corticosteroid therapy and diagnostic scores are essential for diagnostic autoimmune hepatitis.
PRIMITIVE BILIARY CHOLANGITIS - AUTOIMMUNE HEPATITIS OVERLAP SYNDROME: CASE REPORT AN...
Chantelli Razafindrazoto
Andry Rakotozafindrabe

Chantelli Razafindrazoto

and 6 more

July 20, 2020
Overlap syndrome associating primary biliary cholangitis and autoimmune hepatitis remains a rarely studied pathology. The diagnosis is based on diagnostic criteria. The criteria of Chazouillères (Paris criterion) et al were the most used. The combination of UDCA and immunosuppressive helped achieve remission in the majority of cases.

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