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Annals of Dermatology ; : 270-273, 1998.
Article in English | WPRIM | ID: wpr-51034

ABSTRACT

We report a case of myelodysplastic syndrome (MDS) with unique histopathological findings in which numerous infiltrated neutrophils exhibited nuclear segmentation anomalies. In comparison with well-described neutrophilic dermatoses of myelodysplastic syndrome such as Sweets syndrome and pyoderma gangrenosum, this case took a rapid and aggressive clinical course. We suggest that a nuclear segmentation anomaly, pseudo Pelger-Hiiet anomaly, is likely to reflect acute transformation of MDS and can be a poor prognostic marker.


Subject(s)
Myelodysplastic Syndromes , Neutrophils , Pyoderma Gangrenosum , Skin Diseases , Sweet Syndrome
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