T. Kaneki et al., Immunoblastic lymphadenopathy-like T-cell lymphoma complicated by multiplegastrointestinal involvement, J GASTRO, 34(2), 1999, pp. 253-259
We report a rare case of immunoblastic lymphadenopathy (IBL)-like T-cell ly
mphoma complicated by multiple gastrointestinal involvement, which appeared
to be ameliorated by chemotherapy but resulted in perforative peritonitis.
A 66-year-old Japanese woman who had generalized lymphadenopathy and erupt
ions was admitted to our hospital because of bloody stool. Colonoscopic exa
mination revealed hemorrhagic ulcers in the terminal ileum and a saucer-lik
e ulcer in the cecum. Gastrointestinal endoscopy revealed several ulcerativ
e or elevated lesions in stomach and duodenum. Biopsy specimens of these le
sions and of a lymph node showed characteristic histological features of IB
L-like T-cell lymphoma. The initial treatment with prednisolone (PSL) and c
yclophosphamide (CPA) was effective. Six months after the treatment, howeve
r, she developed bloody stool again caused by multiple ulcerative lesions i
n the large intestine. The recurrence of the disease was determined histolo
gically, and four courses of CPA, PSL, vinblastine sulfate and doxorubicin
hydrochloride (CHOP) therapy were administered. One month after completing
the CHOP therapy, she developed intestinal obstruction and then acute perit
onitis resulting from perforation at an ulcer scar in the jejunum. Surgical
treatment was successful, and histological examination demonstrated no lym
phoma cells in the resected specimen, A gastrointestinal perforation should
be recognized as a potential complication of IBL-like T-cell lymphoma, eve
n during remission.