Hemolytic uremic syndrome after high dose chemotherapy with autologous stem cell support. 1995

H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
Academic Medical Centre, University of Amsterdam, Department of Internal Medicine, Amsterdam, The Netherlands.

BACKGROUND Chemotherapy intensification may lead to new forms of toxicity such as hemolytic uremic syndrome. METHODS Three patients are described who developed this complication 4 to 6 months after high dose chemotherapy followed by autologous stem cell support. The literature on this subject is reviewed. RESULTS One patient was conditioned with BEAC (carmustine, etoposide, cytosine arabinoside, and cyclophosphamide) and received autologous bone marrow. The other two underwent triple peripheral stem cell transplantation after conditioning with CTC (carboplatin, cyclophosphamide, and thiotepa). Symptoms were hypertension, microangiopathic hemolytic anemia, thrombocytopenia, and renal insufficiency. One patient had a retinal vein thrombosis. One patient died of a cardiac arrest shortly after the diagnosis was made. The remaining two achieved a partial remission: one with fresh frozen plasma without plasmapheresis and fresh frozen plasma, but improved on high dose intravenous immunoglobulin and vincristine. CONCLUSIONS Hemolytic uremic syndrome is a serious complication of the more intensive chemotherapy made possible by stem cell support. Because of the rapidly growing indications for this approach, an increase in this type of vascular complication is expected.

UI MeSH Term Description Entries
D006973 Hypertension Persistently high systemic arterial BLOOD PRESSURE. Based on multiple readings (BLOOD PRESSURE DETERMINATION), hypertension is currently defined as when SYSTOLIC PRESSURE is consistently greater than 140 mm Hg or when DIASTOLIC PRESSURE is consistently 90 mm Hg or more. Blood Pressure, High,Blood Pressures, High,High Blood Pressure,High Blood Pressures
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D010949 Plasma The residual portion of BLOOD that is left after removal of BLOOD CELLS by CENTRIFUGATION without prior BLOOD COAGULATION. Blood Plasma,Fresh Frozen Plasma,Blood Plasmas,Fresh Frozen Plasmas,Frozen Plasma, Fresh,Frozen Plasmas, Fresh,Plasma, Blood,Plasma, Fresh Frozen,Plasmas,Plasmas, Blood,Plasmas, Fresh Frozen
D012074 Remission Induction Therapeutic act or process that initiates a response to a complete or partial remission level. Induction of Remission,Induction, Remission,Inductions, Remission,Remission Inductions
D002330 Carmustine A cell-cycle phase nonspecific alkylating antineoplastic agent. It is used in the treatment of brain tumors and various other malignant neoplasms. (From Martindale, The Extra Pharmacopoeia, 30th ed, p462) This substance may reasonably be anticipated to be a carcinogen according to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985). (From Merck Index, 11th ed) BCNU,1,3-Bis(2-Chloroethyl)-1-Nitrosourea,BiCNU,FIVB,N,N'-Bis(2-Chloroethyl)-N-Nitrosourea,Nitrumon
D003520 Cyclophosphamide Precursor of an alkylating nitrogen mustard antineoplastic and immunosuppressive agent that must be activated in the LIVER to form the active aldophosphamide. It has been used in the treatment of LYMPHOMA and LEUKEMIA. Its side effect, ALOPECIA, has been used for defleecing sheep. Cyclophosphamide may also cause sterility, birth defects, mutations, and cancer. (+,-)-2-(bis(2-Chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorine 2-Oxide Monohydrate,B-518,Cyclophosphamide Anhydrous,Cyclophosphamide Monohydrate,Cyclophosphamide, (R)-Isomer,Cyclophosphamide, (S)-Isomer,Cyclophosphane,Cytophosphan,Cytophosphane,Cytoxan,Endoxan,NSC-26271,Neosar,Procytox,Sendoxan,B 518,B518,NSC 26271,NSC26271
D003561 Cytarabine A pyrimidine nucleoside analog that is used mainly in the treatment of leukemia, especially acute non-lymphoblastic leukemia. Cytarabine is an antimetabolite antineoplastic agent that inhibits the synthesis of DNA. Its actions are specific for the S phase of the cell cycle. It also has antiviral and immunosuppressant properties. (From Martindale, The Extra Pharmacopoeia, 30th ed, p472) Ara-C,Arabinofuranosylcytosine,Arabinosylcytosine,Cytosine Arabinoside,Aracytidine,Aracytine,Cytarabine Hydrochloride,Cytonal,Cytosar,Cytosar-U,beta-Ara C,Ara C,Arabinoside, Cytosine,Cytosar U,beta Ara C
D005047 Etoposide A semisynthetic derivative of PODOPHYLLOTOXIN that exhibits antitumor activity. Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA. This complex induces breaks in double stranded DNA and prevents repair by topoisomerase II binding. Accumulated breaks in DNA prevent entry into the mitotic phase of cell division, and lead to cell death. Etoposide acts primarily in the G2 and S phases of the cell cycle. Demethyl Epipodophyllotoxin Ethylidine Glucoside,Celltop,Eposide,Eposin,Eto-GRY,Etomedac,Etopos,Etoposide Pierre Fabre,Etoposide Teva,Etoposide, (5S)-Isomer,Etoposide, (5a alpha)-Isomer,Etoposide, (5a alpha,9 alpha)-Isomer,Etoposide, alpha-D-Glucopyranosyl Isomer,Etoposido Ferrer Farma,Exitop,Lastet,NSC-141540,Onkoposid,Riboposid,Toposar,VP 16-213,VP-16,Vepesid,Vépéside-Sandoz,Eto GRY,Etoposide, alpha D Glucopyranosyl Isomer,NSC 141540,NSC141540,Teva, Etoposide,VP 16,VP 16 213,VP 16213,VP16,Vépéside Sandoz,alpha-D-Glucopyranosyl Isomer Etoposide
D005260 Female Females

Related Publications

H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
November 1997, Current opinion in hematology,
H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
December 1992, Oncology (Williston Park, N.Y.),
H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
May 2000, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke,
H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
June 1999, Tecnologica. MAP supplement. Blue Cross and Blue Shield Association. Medical Advisory Panel,
H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
January 2006, Anticancer research,
H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
May 2004, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke,
H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
January 1999, Tecnologica. MAP supplement. Blue Cross and Blue Shield Association. Medical Advisory Panel,
H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
February 1998, Tecnologica. MAP supplement. Blue Cross and Blue Shield Association. Medical Advisory Panel,
H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
April 1996, Annals of medicine,
H van der Lelie, and J W Baars, and S Rodenhuis, and M A van Dijk, and C W de Glas-Vos, and B L Thomas, and R H van Oers, and A E von dem Borne
August 1998, Cancer treatment reviews,
Copied contents to your clipboard!