Pseudotumoral enterocolitis and massive eosinophilia.

Abstract:

:We report a seven year history of a 23 year old woman born in the Antilles, with pseudotumoral enterocolitis and massive eosinophilia. In 1973 she developed a haemorrhagic colitis with massive peripheral eosinophilia of up to 60000/mm3. Medical treatment, mainly corticosteroids, failed to control the disease. The patient temporarily improved after colectomy and remained in remission for two years. In 1978 the disease recurred in the rectum and small intestine with formation of tumour-like granulomata and massive infiltration by eosinophils, unresponsive to corticosteroids. Intestinal blood and protein loss continued until death seven years after onset. In spite of exhaustive investigation, no parasites, allergens, or other aetiological agents could be found. As only the gut was infiltrated, the hypereosinophilic syndrome could be excluded. The enterocolitis here described does not correspond to an eosinophilic gastroenteritis, nor to other known inflammatory bowel diseases and to our knowledge has not been reported previously.

journal_name

Gut

journal_title

Gut

authors

Malè PJ,de Toledo F,Widgren S,de Peyer R,Berthoud S

doi

10.1136/gut.24.4.345

subject

Has Abstract

pub_date

1983-04-01 00:00:00

pages

345-50

issue

4

eissn

0017-5749

issn

1468-3288

journal_volume

24

pub_type

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