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ADRENAL MYELOLIPOMA - REPORT OF 15 PATIENTS

MIRAN BEZJAK orcid id orcid.org/0000-0001-6235-1162 ; Medicinski fakultet, Sveučilište u Zagrebu,Zagreb, Hrvatska
PATRICIJA SESAR ; Odjel za patologiju, Opća bolnica “Dr Ivo Pedišić”, Sisak, Hrvatska
MONIKA ULAMEC orcid id orcid.org/0000-0002-4843-8154 ; Klinički zavod za patologiju Ljudevit Jurak, Klinički bolnički centar Sestre milosrdnice, Zavod za patologiju, Medicinski fakultet, Sveučilište u Zagrebu, Zagreb, Hrvatska
IVANA PAVIĆ ; Klinički zavod za patologiju Ljudevit Jurak, Klinički bolnički centar Sestre milosrdnice, Zagreb, Hrvatska
AUGUST MIJIĆ ; Klinika za kirurgiju, Klinički bolnički centar Sestre milosrdnice, Zagreb, Hrvatska
BORISLAV SPAJIĆ ; Klinika za urologiju, Klinički bolnički centar Sestre milosrdnice, Zagreb, Hrvatska
BOŽO KRUŠLIN orcid id orcid.org/0000-0002-0480-1687 ; Klinički zavod za patologiju Ljudevit Jurak, Klinički bolnički centar Sestre milosrdnice, Zavod za patologiju, Medicinski fakultet, Sveučilište u Zagrebu, Zagreb, Hrvatska


Puni tekst: hrvatski pdf 1.008 Kb

str. 255-258

preuzimanja: 2.617

citiraj


Sažetak

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.

Ključne riječi

adrenal gland; myelolipoma

Hrčak ID:

113386

URI

https://hrcak.srce.hr/113386

Datum izdavanja:

14.1.2014.

Podaci na drugim jezicima: hrvatski

Posjeta: 5.019 *