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ADRENAL MYELOLIPOMA - REPORT OF 15 PATIENTS

MIRAN BEZJAK orcid id orcid.org/0000-0001-6235-1162 ; School of Medicine, University of Zagreb, Zagreb, Croatia
PATRICIJA SESAR ; Department of Pathology, Dr Ivo Pedišić General Hospital, Sisak, Croatia
MONIKA ULAMEC orcid id orcid.org/0000-0002-4843-8154 ; Ljudevit Jurak University Department of Pathology, Sestre milosrdnice University Hospital Center, Institute of Pathology, School of Medicine, University of Zagreb, Zagreb, Croatia
IVANA PAVIĆ ; Ljudevit Jurak University Department of Pathology, Sestre milosrdnice University Hospital Center, Zagreb, Croatia
AUGUST MIJIĆ ; Department of Surgery, Sestre milosrdnice University Hospital Center, Zagreb, Croatia
BORISLAV SPAJIĆ ; Department of Urology, Sestre milosrdnice University Hospital Center, Zagreb, Croatia
BOŽO KRUŠLIN orcid id orcid.org/0000-0002-0480-1687 ; Ljudevit Jurak University Department of Pathology, Sestre milosrdnice University Hospital Center, Institute of Pathology, School of Medicine, University of Zagreb, Zagreb, Croatia


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Abstract

Myelolipoma is a rare, benign, non-functioning tumor most frequently located in the adrenal cortex. It consists of mature fatty tissue with components of hematopoietic tissue in different proportions. There are certain ambiguities related to the diagnosis and therapy of myelolipoma, and it is therefore important to keep in view all the aspects of the lesion and the circumstances in which it develops. This paper presents a series of 15 patients with myelolipoma diagnosed at the Ljudevit Jurak Department of Pathology, Sestre milosrdnice University Hospital Center. Out of 15 patients, 10 were men (one of them with bilateral tumor) aged 41 to 73, and 5 were women aged 51 to 54. Macroscopically, the tumors were oval, encapsulated, yellowish, soft masses located in the adrenal glands. The diameter of the tumors ranged between 0.5 and 13.9 cm. Microscopically, they consisted of multiplied mature adipose cells combined with myeloid tissue composed largely of megakaryocytes, erythroid cells and lymphocytes. In all patients, the postoperative course was uneventful with no recurrences.

Keywords

adrenal gland; myelolipoma

Hrčak ID:

113386

URI

https://hrcak.srce.hr/113386

Publication date:

14.1.2014.

Article data in other languages: croatian

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