Literature DB >> 15716662

Hereditary vacuolar internal anal sphincter myopathy causing proctalgia fugax and constipation: a new case contribution.

Fernando de la Portilla1, Juan José Borrero, Enrique Rafel.   

Abstract

Hereditary anal sphincter myopathy is rare. We present a family with one affected member with proctalgia fugax, constipation and internal anal sphincter hypertrophy. Ultrastructural findings show vacuolization of smooth muscle cells without the characteristic polyglucosan inclusion. Further relief of symptoms was obtained using an oral calcium antagonist. Based on clinical presentation, endosonography and morphological findings, we consider our case is a histological variant of the vacuolar myopathy originally described.

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Year:  2005        PMID: 15716662     DOI: 10.1097/00042737-200503000-00016

Source DB:  PubMed          Journal:  Eur J Gastroenterol Hepatol        ISSN: 0954-691X            Impact factor:   2.566


  3 in total

1.  Proctalgia fugax, an evidence-based management pathway.

Authors:  Santhini Jeyarajah; Andre Chow; Paul Ziprin; Henry Tilney; Sanjay Purkayastha
Journal:  Int J Colorectal Dis       Date:  2010-06-16       Impact factor: 2.571

2.  Clinical examination remains more important than anorectal function tests to identify treatable conditions in women with constipation.

Authors:  T J Lam; R J F Felt-Bersma
Journal:  Int Urogynecol J       Date:  2012-05-23       Impact factor: 2.894

3.  Proctalgia and constipation secondary to hypertrophic polyglucosan inclusion body myopathy of the internal anal sphincter: a case report.

Authors:  Ioanna G Panagiotopoulou; Richard Miller; Michael P Powar; James Y H Chan; R Justin Davies
Journal:  J Med Case Rep       Date:  2018-10-24
  3 in total

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