Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Primary myelofibrosis

A rare myeloproliferative neoplasm characterized by stem-cell derived clonal over proliferation of mature myeloid lineages, such as erythrocytes, leukocytes, and megakaryocytes, with variable degrees of megakaryocyte atypia, associated with reticulin and/or collagen bone marrow fibrosis, osteosclerosis, ineffective erythropoiesis, angiogenesis, extramedullary hematopoiesis, and abnormal cytokine expression.

Hepatic failure

Total: 1

(per page)

PMID (PMCID)
15621770	MALE	Middle Aged
	Fatal hepatic failure associated with graft rejection following reduced-intensity stem-cell transplantation for chronic idiopathic myelofibrosis (CIMF).
	Miyakoshi S, Kami M, Kishi Y, Murashige N, Yuji K, Kusumi E, Matsumura T, Onishi Y, Kobayashi K, Kim SW, Hamaki T, Takaue Y, Taniguchi S. Leuk Lymphoma. 2004;45(12):2513-6.
	Fatal hepatic failure associated with graft rejection following reduced-intensity stem-cell transplantation for chronic idiopathic myelofibrosis (CIMF).