Literature DB >> 15491437

Whipple's disease presenting with symmetrical panniculitis.

A C Friedmann1, G K Perera, A Jayaprakasam, I Forgacs, J R Salisbury, D Creamer.   

Abstract

Specific cutaneous involvement in Whipple's disease is extremely rare. The condition usually runs a chronic course, with symptoms preceding diagnosis by years or even decades. We report a 44-year-old man who presented with a rapid onset of progressive, extensive, symmetrical plaques of panniculitis affecting the inner thighs and forearms. He had accompanying large joint arthritis and was profoundly anaemic. Biopsy of the subcutis revealed a florid septal panniculitis with infiltration of the septa by foamy macrophages containing intracellular granules that stained strongly with periodic acid-Schiff reagent. A similar but more intense infiltrate was seen in the small bowel lamina propria, and a diagnosis of Whipple's disease was made. Symmetrical panniculitis has not previously been reported as a manifestation of Whipple's disease.

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Year:  2004        PMID: 15491437     DOI: 10.1111/j.1365-2133.2004.06179.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  3 in total

1.  [Rare erosive arthritis and dermatitis syndrome in Whipple's disease].

Authors:  M Krusche; D Boro; J Bertolini; I Kötter
Journal:  Z Rheumatol       Date:  2019-03       Impact factor: 1.372

2.  Eosinophilic vasculitis: a rare presentation of Whipple's disease.

Authors:  Waleed Al-Hamoudi; Fadi Habbab; Carmine Nudo; Ayoub Nahal; Kenneth Flegel
Journal:  Can J Gastroenterol       Date:  2007-03       Impact factor: 3.522

Review 3.  Clinical Manifestations, Treatment, and Diagnosis of Tropheryma whipplei Infections.

Authors:  Ruben A V Dolmans; C H Edwin Boel; Miangela M Lacle; Johannes G Kusters
Journal:  Clin Microbiol Rev       Date:  2017-04       Impact factor: 26.132

  3 in total

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