Summary:Bone marrow transplant-associated thrombotic microangiopathy (BMT-TM), usually associated with thrombocytopenia, microangiopathic haemolytic anaemia (MAHA) and renal insufficiency, has been reported to occur approximately 5-6 months after BMT. We report a case of relapsed malignant lymphoma complicated by BMT-TM of hyperacute onset, which has never been described in the literature. Our patient, a 52-yearold male, developed MAHA with gross haematuria, thrombocytopenia, lactate dehydrogenase elevation and renal insufficiency 2 days after autologous PBSC transplantation following high-dose chemotherapy. Supportive treatment, ie glucocorticoid, fresh frozen plasma and haemodiafiltration were given, and thereafter the BMT-TM gradually improved. In heavily pretreated patients, caution should be exercised for possible occurrence of the BMT-TM of hyperacute onset. Keywords: thrombotic microangiopathy; hyperacute onset; PBSCT; high-dose chemotherapy Thrombotic microangiopathy (TM) in association with BMT (BMT-TM) has been reported by several investigators. 1,2 In the setting of allogeneic BMT, not only conditioning therapy, but also CsA, GVHD and cytomegalovirus (CMV) infection are incriminated as possible factors in the pathogenesis of BMT-TM. 1,2 In autologous BMT, conditioning therapy has been proposed as a cause. 2 Although conditioning-associated TM is generally thought to occur approximately 5-6 months after BMT, 2 we report a case of hyperacute onset (during high-dose chemotherapy (HDC) ) TM following autologous PBSC transplantation (PBSCT). Such hyperacute onset BMT-TM has never been reported in the literature.Correspondence: K Tobinai, Department of Medical Oncology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-ku, Tokyo 104, Japan Received 3 October 1997; accepted 28 January 1998
Case reportA 52-year-old man was diagnosed as having stage IV peripheral T cell lymphoma involving retroperitoneal lymph nodes, liver, spleen, and bone marrow in May 1994. He received several regimens of combination chemotherapy (MACOP-B, consisting of methotrexate, doxorubicin, cyclophosphamide, vincristine, prednisolone and bleomycin; CHOP, consisting of cyclophosphamide, doxorubicin, vincristine and prednisolone; CHOP-bleo, consisting of CHOP with bleomycin), which produced some response, but his disease progressed and he was referred to our hospital in April 1996. Salvage chemotherapy consisting of etoposide, methylprednisolone, high-dose cytarabine and cisplatin (ESHAP) 3 produced a partial response. The harvested PBSC which were enriched for CD34 + cells were cryopreserved as previously described. 4 Organ function remained within normal limits before the patient received HDC with PBSCT.In August 1996, he was treated with high-dose carboplatin (200 mg/m 2 /day (total dose 1000 mg/m 2 ) ), cyclophosphamide (1200 mg/m 2 /day (total dose 6000 mg/m 2 ) ), etoposide (250 mg/m 2 /day (total dose 1250 mg/m 2 ) ) and dexamethazone (40 mg/day (total dose 200 mg) ) on 5 consecutive days (days Ϫ7 to Ϫ3). Vomiting and diarrho...