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[Renal extramedullary hematopoietic tumor revealing a hereditary spherocytosis in an adult patient].

作者信息

Boucher A, Puech P, Kharroubi D, Boyer T, Lefèvre G, Charpentier A, Cliquennois M, Rose C

机构信息

Service d'onco-hématologie, hôpital Saint-Vincent-de-Paul, université catholique de Lille, université Lille Nord de France, 59000 Lille, France.

Service de radiologie, CHRU de Lille, université Lille Nord de France, 59000 Lille, France.

出版信息

Rev Med Interne. 2015 Dec;36(12):848-53. doi: 10.1016/j.revmed.2015.02.007. Epub 2015 Mar 18.

Abstract

INTRODUCTION

Myelolipomas and extramedullary hematopoietic tumors are uncommon benign tumors. They are variably composed of mature adipose tissue and hematopoietic tissue. Myelolipoma is usually observed in the adrenal gland and extramedullary hematopoietic tumors in the liver and spleen but may occasionally be found within solid tumors.

CASE REPORT

A 62-year-old man without previous haematological history presented with a voluminous solitary bilateral renal tumor. Contrast-enhanced ultrasound CT-scan and scintigraphy with technetium-99m-nanocolloid and indium-111-chloride bone marrow were highly suggestive of extramedullary hematopoietic tumor. CT-guided biopsy suggested a diagnosis of myelolipoma. An atypical hereditary spherocytosis, undiagnosed until now, was demonstrated.

CONCLUSION

We report, for the first time to our knowledge, a border form between extramedullary hematopoiesis tumor and myelolipoma of renal localisation revealing a hereditary spherocytosis in an adult patient.

摘要

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