Literature DB >> 25000468

Diffuse hemorrhagic colitis in a patient with dyskeratosis congenita after nonmyeloablative allogeneic hematopoietic stem cell transplantation.

Karoline Ehlert1, Claudia Rossig, Andreas H Groll, Torsten Beyna, Birgit Froehlich, Heribert Juergens.   

Abstract

Dyskeratosis congenita (DC) is a rare inherited disorder characterized by reticular skin pigmentation, oral cavity leukoplakia, and nail dystrophy. Bone marrow failure in DC can only be cured by allogeneic hematopoietic stem cell transplantation (HSCT). After a nonmyeloablative, matched unrelated donor transplant, the 21-year-old patient experienced severe lower gastrointestinal tract hemorrhage caused by diffuse colitis. The etiology remained unclear. Diffuse colitis with life-threatening hemorrhage has now been reported in 3 DC patients after unrelated allogeneic HSCT. To identify the underlying causes and the disease-specific risks, and to allow for prevention and/or optimal management, data should be prospectively collected.

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Year:  2015        PMID: 25000468     DOI: 10.1097/MPH.0000000000000208

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  1 in total

1.  Fatal Hemorrhagic Gastrointestinal Angioectasia after Bone Marrow Transplantation for Dyskeratosis Congenita.

Authors:  Jin Imai; Takayoshi Suzuki; Marie Yoshikawa; Makiko Dekiden; Hirohiko Nakae; Fumio Nakahara; Shingo Tsuda; Hajime Mizukami; Jun Koike; Muneki Igarashi; Hiromasa Yabe; Tetsuya Mine
Journal:  Intern Med       Date:  2016-12-01       Impact factor: 1.271

  1 in total

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