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An unusual case of hereditary transthyretin‐related amyloidosis and ulcerative colitis in a young Indian girl
Author(s) -
Sharma Vishal,
Sharma Pankaj,
Singh Minu,
Agarwala Roshan,
Prasad Kaushal K,
Mandavdhare Harshal S,
Dutta Usha,
Bhatia Prateek
Publication year - 2020
Publication title -
jgh open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.546
H-Index - 8
ISSN - 2397-9070
DOI - 10.1002/jgh3.12206
Subject(s) - medicine , amyloidosis , ulcerative colitis , transthyretin , diarrhea , constipation , dysphagia , gastroenterology , pediatrics , disease , surgery
Hereditary transthyretin (TTR) amyloidosis is a multisystem disorder caused by extracellular amyloid deposition, usually presenting with neurological and cardiovascular involvement. Gastrointestinal involvement, if present, is usually in the form of motility symptoms like diarrhea, constipation, or diarrhea alternating with constipation. Presentations mimicking ulcerative colitis without other system involvement are rare. Here we present a case of a young female from northern India, who presented with blood‐admixed diarrhea without any feature of any other system involvement. She was diagnosed and treated as ulcerative colitis for two years with ambivalent response, although the compliance to therapy was also poor. She was re‐evaluated when she presented with recurrence of symptoms and new onset dysphagia. On evaluation, she was diagnosed as hereditary transthyrtetin related amyloidosis.

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