N. Bhagwati et al., FULMINANT METASTATIC MELANOMA COMPLICATED BY A MICROANGIOPATHIC HEMOLYTIC-ANEMIA, Hematopathology and molecular hematology, 11(2), 1998, pp. 101-108
A 34-year-old male acutely presented with widely disseminated malignan
t melanoma, a microangiopathic hemolytic anemia, and disseminated intr
avascular coagulation Although the patient had a history of incense ch
ildhood exposure to ultraviolet light and an occupational exposure to
organic dyes, he had no history of a precursor skin lesion. The histop
athology of the patient's bone marrow revealed sheets of malignant cel
ls immunoreactive with S-100, HMB-45, and vimentin and also staining p
ositively for melanin. A bone marrow aspirate revealed myeloid precurs
ors filled with melanin-bearing vacuoles. Immunophenotypic analysis of
the patient's bone marrow by flow cytometry revealed a paucity of hem
atopoietic cells. A karyotypic analysis of the patient's tumor cells d
emonstrated an abnormal hypertriploid composite clone characterized by
multiple numerical and structural abnormalities. Although the patient
was treated aggressively with transfusional support, heparin, and che
motherapy, he expired 3 weeks after diagnosis. This is the first recog
nized case of metastatic melanoma occurring in association with a micr
oangiopathic hemolytic anemia.