Cho Min Ho, Mandaliya Rohan, Liang John, Patel Mitesh
Department of Medicine, MedStar Washington Hospital Center Division of Gastroenterology and Hepatology, MedStar Georgetown University Hospital Department of Pathology, MedStar Washington Hospital Center, Washington, DC.
Medicine (Baltimore). 2018 Apr;97(15):e0337. doi: 10.1097/MD.0000000000010337.
Extra-adrenal myelolipoma in the presacral area often raises a concern for liposarcoma because they have similar radiologic features.
A 70-year-old woman with multiple abdominal surgeries in the past presented with persistent lower abdominal pain and anemia. A presacral mass, found on a pelvic magnetic resonance image (MRI), was suspicious of liposarcoma, as it is the most common fat containing mass in the presacral area. It is often difficult to make a diagnosis of myelolipoma just based on the radiological studies, which necessitates a histopathologic examination of the resected mass for a definitive diagnosis.
Myelolipoma is an encapsulated, benign tumor containing mature adipocytes and hematologic cells. Most of the patients with myelolipoma remain asymptomatic but continued growth of tumor without local invasion can lead to compression of nearby structures, causing persistent pain.
Asymptomatic patients do not require intervention but surgical resection is indicated for persistent pain or hemorrhage inside the tumor. Our patient had 2 indications for surgery - persistent pain as well as a provisional diagnosis of liposarcoma. After the surgical resection, pelvic pain was resolved, and a diagnosis of myelolipoma was made based on histopathologic examination.
Patient was reassured that it was myelolipoma, a benign tumor, not requiring subsequent surveillance for recurrence.
Despite advancement in imaging techniques, and knowledge of the radiological features of myelolipoma, it still remains as a challenge for clinicians to make the distinction between liposarcoma and myelolipoma only based on diagnostic radiology. Although myelolipoma is a benign tumor, if patient suffers from persistent pain due to local mass effect, surgical resection is required.
骶前区域的肾上腺外髓脂肪瘤常引发对脂肪肉瘤的担忧,因为它们具有相似的放射学特征。
一名70岁女性,既往有多次腹部手术史,出现持续性下腹痛和贫血。盆腔磁共振成像(MRI)发现骶前肿物,怀疑为脂肪肉瘤,因为它是骶前区域最常见的含脂肪肿物。仅基于放射学检查往往难以诊断髓脂肪瘤,这就需要对切除的肿物进行组织病理学检查以明确诊断。
髓脂肪瘤是一种包膜完整的良性肿瘤,含有成熟的脂肪细胞和血液细胞。大多数髓脂肪瘤患者无症状,但肿瘤持续生长且无局部侵犯可导致压迫附近结构,引起持续性疼痛。
无症状患者无需干预,但对于持续性疼痛或肿瘤内出血则需手术切除。我们的患者有两个手术指征——持续性疼痛以及脂肪肉瘤的初步诊断。手术切除后,盆腔疼痛缓解,根据组织病理学检查确诊为髓脂肪瘤。
患者得知是髓脂肪瘤,一种良性肿瘤,无需后续监测复发情况,感到安心。
尽管成像技术有所进步,且对髓脂肪瘤的放射学特征有所了解,但临床医生仅基于诊断性放射学来区分脂肪肉瘤和髓脂肪瘤仍然是一项挑战。虽然髓脂肪瘤是良性肿瘤,但如果患者因局部肿块效应而遭受持续性疼痛,则需要手术切除。