Development of in situ melanoma after allogeneic bone marrow transplantation in Griscelli syndrome type II

被引：2
作者：
Koese, Osman [1 ]
Kuerekci, Ahmet Emin
Safali, Muekerrem
Akin, Ridvan
Koeseoglu, Vedat
Tezcan, Ilhan
机构：
[1] Gulhane Mil Med Acad, Dept Dermatol, TR-06018 Ankara, Turkey
[2] Gulhane Mil Med Acad, Dept Pediat, Ankara, Turkey
[3] Gulhane Mil Med Acad, Dept Pathol, Ankara, Turkey
[4] Univ Hacettepe, Fac Med, Dept Pediat, Div Immunol, Ankara, Turkey
来源：
PEDIATRIC TRANSPLANTATION | 2007年 / 11卷 / 07期
关键词：
Griscelli syndrome; childhood melanoma; allogeneic bone marrow transplantation;
D O I：
10.1111/j.1399-3046.2007.00758.x
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
GS is an uncommon autosomal recessive disorder characterized by pigmentary dilution of the skin and hair and in most patients by abnormal regulation of the immune system. Childhood melanoma is rare in the pediatric population. The best prognosis is achieved with early diagnosis and definitive surgical excision of melanoma. We report a case of a patient with GS type II and melanoma who was successfully treated by allogeneic bone marrow transplantation and surgical excision of the melanoma.
引用
收藏
页码：792 / 795
页数：4
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