Literature DB >> 10979208

Myelodysplastic syndrome terminating in erythropoietic protoporphyria after 15 years of aplastic anemia.

T Shirota1, H Yamamoto, S Hayashi, H Fujimoto, Y Harada, T Hayashi.   

Abstract

The authors report a case of aplastic anemia in which refractory anemia, a subtype of myelodysplastic syndrome (MDS), developed 15 years after the onset and was subsequently followed by erythropoietic protoporphyria (EPP). Defects of stem cells in MDS are thought to be responsible for the disturbance of the heme biosynthetic pathway, leading to the development of EPP.

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Year:  2000        PMID: 10979208

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  3 in total

1.  Severe aplastic anemia in a patient with erythropoietic protoporphyria successfully treated by avatrombopag.

Authors:  Ziming Jiang; Xianyong Jiang; Miao Chen
Journal:  Ann Hematol       Date:  2021-11-26       Impact factor: 3.673

2.  Photosensitivity and acute liver insufficiency in late-onset erythropoietic protoporphyria with a chromosome 18q abnormality.

Authors:  Yuka Oshikawa; Satoshi Fukushima; Taiga Miyake; Takeshi Kawaguchi; Kenta Motomura; Yasuhiro Nakashima; Kenichi Nakamura; Masatoshi Jinnin; Hironobu Ihn
Journal:  Case Rep Dermatol       Date:  2012-07-10

3.  From the dermatologikum hamburg: quiz.

Authors:  Wendemagegn E Yeshanehe; Rajalakshmi Tirumalae; Almut Böer-Auer
Journal:  Dermatol Pract Concept       Date:  2012-10-31
  3 in total

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