Home > Journals > Minerva Chirurgica > Past Issues > Minerva Chirurgica 2000 July-August;55(7-8) > Minerva Chirurgica 2000 July-August;55(7-8):559-64

CURRENT ISSUE
 

ARTICLE TOOLS

Reprints

MINERVA CHIRURGICA

A Journal on Surgery


Indexed/Abstracted in: EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 1,115


eTOC

 

CASE REPORT  


Minerva Chirurgica 2000 July-August;55(7-8):559-64

Copyright © 2000 EDIZIONI MINERVA MEDICA

language: Italian

A case of presacral myelolipoma

Zanon C., Bortolini M., Bo P., Sandrucci S., Trombetta F., Deandrea M., Mussa A.


PDF  


Myelolipoma is a rare benign pathology whose pathogenesis is still unclear. It is most frequently localised in the adrenal gland, followed by the presacral region, mediastinum, and perirenal and hepatic region. It varies in size from a few millimetres to several centimetres. The lesion is usually capsulated, detachable from the surrounding tissues and hypovascularised. In histological terms, it is composed of lipomatous and hematopoietic tissues. A 65-year-old female patient was referred to our unit after the finding of a nonbiopsied, pelvic mass during earlier surgery. The patient was in considerable pain owing to the extrinsic compression of the mass on abdominal and pelvic organs. Preoperative tests confirmed the presence of a voluminous presacral neoformation that appeared to have a possible medullary origin (chordoma or schwannoma). During surgery, the lesion was found to be capsulated and mainly adherent to the rectus. Histological analysis confirmed the myelolipomatous nature of the lesion. A review of 21 cases reported in the literature is presented.

top of page

Publication History

Cite this article as

Corresponding author e-mail