Sclerosing Lipogranulomatosis: Its Several Abdominal Syndromes
- 1 June 1967
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Surgery
- Vol. 94 (6), 803-810
- https://doi.org/10.1001/archsurg.1967.01330120057012
Abstract
SEVERAL reports concerning chronic inflammatory infiltrations of the small bowel mesentery and retroperitoneum have been published. Xanthogranulomatous obstruction of the colon,1 sclerosing retroperitonitis with ureteral obstruction,2 and isolated mesenteric panniculitis3 would at first appear to be distinctly separate pathological entities. It is our opinion, however, that each represents a different symptom complex resulting from the same nonspecific tissue reaction. The process seems to begin with a fatty tissue injury which results in a granulomatous cellular reaction followed by fibrosis. The resulting clinical picture is determined by the envelopment and gradual narrowing of the tubular structures that lie within the mass. Gross and microscopic descriptions of tissue obtained from patients with these several afflictions have shown consistent similarities, suggesting that clinical differences are chiefly due to location, extent, and duration of the process. We postulate that these and similar syndromes are manifestations of sclerosing lipogranulomatosis. Report of CasesThis publication has 7 references indexed in Scilit:
- Intestinal lipodystrophy (Whipple's disease); the immediate and prolonged effect of antibiotic therapyJAMA, 1966
- Vascular complications with use of methysergideArchives of Internal Medicine, 1966
- Severe peripheral arterial constriction, acute ischemia of lower extremity with use of methysergide and ergotamineArchives of Internal Medicine, 1966
- Retroperitoneal Fibrosis—Two Unusual CasesArchives of Surgery, 1964
- Mesenteric PanniculitisJAMA, 1963
- SYSTEMIC NODULAR PANNICULITIS1953
- Retroperitoneal XanthogranulomaThe American Journal of Cancer, 1935