CHURG-STRAUSS-SYNDROME (ALLERGIC GRANULOMATOUS ANTIITIS) WITH MULTIPLE PERFORATING ULCERS OF THE SMALL-INTESTINE, MULTIPLE ULCERS OF THE COLON, AND MONONEURITIS MULTIPLEX
M. Kurita et al., CHURG-STRAUSS-SYNDROME (ALLERGIC GRANULOMATOUS ANTIITIS) WITH MULTIPLE PERFORATING ULCERS OF THE SMALL-INTESTINE, MULTIPLE ULCERS OF THE COLON, AND MONONEURITIS MULTIPLEX, Journal of gastroenterology, 29(2), 1994, pp. 208-213
A case of Churg-Strauss syndrome with multiple perforations of the sma
ll intestine is described. A 31-year-old woman was admitted with a com
plaint of epigastric pain. She had a history of bronchial asthma. One
week before admission, white blood cell count was 20 800/mm(3) with 59
% eosinophils. Neurological examination on admission disclosed mononeu
ritis multiplex with paresthesia in both the lower and upper extremiti
es. At colonoscopy, there were scattered aphthous ulcers in the colon.
Ophthalmological examination revealed allergic conjunctivitis. After
admission, hypereosinophilia increased to as high as 36 000/mm(3). Ora
l administration of prednisolone (60 mg/day) was begun. On the 3rd day
of the treatment, the eosinophil count decreased dramatically, to 400
/mm(3), while severe abdominal pain developed. Since abdominal X-ray h
im revealed free air in the abdominal cavity, emergency laparotomy was
performed and multiple intestinal ulcers with perforations were found
. Partial ileectomy was performed. Pathological findings of the resect
ed specimen were interpreted as a necrotizing angiitis with extravascu
lar granuloma. Since the operation, the patient has been asymptomatic,
except for neurological symptoms. Hypereosinophilia has decreased wit
hout treatment to counts averaging 270/mm(3), within 3 months. On the
basis of the clinical features and histopathological findings, a diagn
osis of Churg-Strauss syndrome was established.