Yergin Celeste G, Chang Michael, Thomas Ryan M
University of Florida College of Medicine, Gainesville, FL, USA.
Section of Pathology, North Florida/South Georgia Veterans Health System, Gainesville, FL, USA.
Int J Surg Case Rep. 2022 Mar;92:106889. doi: 10.1016/j.ijscr.2022.106889. Epub 2022 Mar 1.
Lipoblastoma-like tumors are rare tumors that can be confused with lipoblastomas and liposarcomas but have distinct characteristics. This tumor has previously been identified in the vulva of females, and recently in isolated cases of young males. Given its rarity, we present an instance of this tumor in an older man, demonstrating that this pathology is not limited to a specific age or sex, and surgeons and pathologists must be aware of it in their differential.
A 58-year-old male presented for evaluation of an enlarging mass in his right gluteal cleft. Prior to referral for surgical evaluation, the patient underwent an ultrasound-guided biopsy of the mass. Histologically, the tumor was a low-grade cellular spindle cell neoplasm in a fibrous to myxoid stroma. Immunohistochemical and molecular workup ruled out several malignant mesenchymal neoplasms, including myxoid liposarcoma, dedifferentiated liposarcoma, melanoma, low-grade fibromyxoid sarcoma, and sarcomatoid carcinoma. The patient initially declined surgery, but the mass continued to grow, and excision was chosen given the uncertain pathology. The tumor was resected with negative margins and histologically characterized as a "lipoblastoma-like lesion", with features of a myxoid liposarcoma and spindle cell lipoma. Seven months post-resection, there were no signs of recurrence or metastasis.
Despite radiologic and pathologic similarities to malignant lipomatous tumors, lipoblastoma-like tumors are benign and have a good prognosis.
Clinicians should be aware of this entity despite its rarity as resection with negative margins is curative and may be needed to rule out more aggressive tumors.
脂肪母细胞瘤样肿瘤是一种罕见肿瘤,可与脂肪母细胞瘤和脂肪肉瘤相混淆,但具有独特特征。此前已在女性外阴部发现该肿瘤,最近在少数年轻男性病例中也有发现。鉴于其罕见性,我们报告一例发生在老年男性的该肿瘤病例,表明这种病理情况不限于特定年龄或性别,外科医生和病理学家在鉴别诊断时必须对此有所认识。
一名58岁男性因右侧臀沟肿物增大前来评估。在转诊进行手术评估之前,患者接受了肿物的超声引导下活检。组织学上,肿瘤是一种位于纤维性至黏液样基质中的低级别细胞性梭形细胞瘤。免疫组化和分子检查排除了几种恶性间叶性肿瘤,包括黏液样脂肪肉瘤、去分化脂肪肉瘤、黑色素瘤、低级别纤维黏液样肉瘤和肉瘤样癌。患者最初拒绝手术,但肿物持续增大,鉴于病理情况不明,遂选择切除。肿瘤切除后切缘阴性,组织学特征为“脂肪母细胞瘤样病变”,具有黏液样脂肪肉瘤和梭形细胞脂肪瘤的特征。切除术后七个月,无复发或转移迹象。
尽管脂肪母细胞瘤样肿瘤在影像学和病理学上与恶性脂肪瘤性肿瘤相似,但它是良性的,预后良好。
尽管该肿瘤罕见,但临床医生应予以关注,因为切缘阴性的切除可治愈疾病,且可能需要切除以排除更具侵袭性的肿瘤。