Janin A, Nelken B, Dufour S, Sault M C, Taboureau O, Zandecki M, Gosselin B
Department of Pathology, Hôpital Calmette, Lille, France.
Am J Pediatr Hematol Oncol. 1988 Winter;10(4):319-22. doi: 10.1097/00043426-198824000-00010.
A 4-month-old infant was admitted with a monoblastic infiltration of the skin associated with osteosclerosis. Both lesions spontaneously disappeared within a few months, but 2 years later, a monoblastic leukemia occurred that was associated with marked skin erythema and myelofibrosis. Skin and bone marrow specimens showed a monoblastic infiltration with numerous intermingled mast cells of normal appearance. Whether myelofibrosis was a feature of a systemic mastocytosis or of the leukemic process is discussed in this case.
一名4个月大的婴儿因皮肤单母细胞浸润伴骨硬化入院。两种病变在几个月内均自发消失,但2年后发生了单母细胞白血病,伴有明显的皮肤红斑和骨髓纤维化。皮肤和骨髓标本显示单母细胞浸润,伴有许多外观正常的肥大细胞相互混杂。在本病例中讨论了骨髓纤维化是系统性肥大细胞增多症的特征还是白血病过程的特征。