Hibernoma
Synopsis

Hibernomas tend to present as painless, slow-growing masses that are firm, mobile, and nontender to palpation. They are well-defined, encapsulated, hypervascular lesions that typically range in diameter from 5-10 cm but may grow to larger than 20 cm. Hibernomas have no sex predilection and tend to occur in adults during middle age, although cases have been documented across ages. There are 4 distinct pathologic variants of hibernomas: typical, myxoid, spindle cell, and lipoma-like. Each variant can be found intermuscularly, intramuscularly, or subcutaneously. Variants are not readily distinguishable clinically or on imaging and require histology for distinction.
Hibernomas are not considered life-threatening and only manifest symptoms secondary to compression of adjacent structures. While often slow growing and asymptomatic, patients may present with rapid tumor growth, fever, and weight loss. There are no reported cases of malignant transformation, recurrence, or metastatic spread after complete excision. Accurate preoperative diagnosis is critical in reducing patient anxiety and guiding proper surgical and surveillance strategy.
There have been speculations about an association between hibernomas and multiple endocrine neoplasia type 1 (MEN1) as there have been a few case reports of hibernoma occurring in patients with MEN1.
Codes
D17.9 – Benign lipomatous neoplasm, unspecified
SNOMEDCT:
404064001 – Hibernoma
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Last Updated:11/12/2020