Pediatric hyperfibrotic myelodysplasia: An unusual clinicopathologic entity

Satyajit Sahu*, Samir S. Shah, Alok Srivastava, David Dennison, Mammen Chandy

*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلةمراجعة النظراء

4 اقتباسات (Scopus)

ملخص

This study is presented to highlight a rare pediatric bone marrow pathology in which features of bone marrow dysplasia coexist with severe fibrosis in a clinical setting of fever, anemia, and organomegaly. Fourteen children (nine males, five females) clinically presented with fever, anemia, and hepatosplenomegaly. Extensive bone marrow fibrosis with dysplastic features was seen in their marrow precursor cells. Peripheral blood smears showed teardrop poikilocytes, thrombocytopenia, and occasional blasts. In conclusion, pediatric hyperfibrotic myelodysplasia is a distinct clinicopathologic entity. Myeloproliferative and dysmyelopoietic syndromes are complex disorders that are interrelated and not always easily diagnosed only on morphologic grounds.

اللغة الأصليةEnglish
الصفحات (من إلى)133-139
عدد الصفحات7
دوريةPediatric Hematology and Oncology
مستوى الصوت14
رقم الإصدار2
المعرِّفات الرقمية للأشياء
حالة النشرPublished - 1997
منشور خارجيًانعم

ASJC Scopus subject areas

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