Amankwah Samuel, Luzuriaga Maria, Denning Krista, Lawrence Logan
Marshall University, Department of Endocrinology, Huntington, West Virginia.
Marshall University, Department of Pathology, Huntington, West Virginia.
AACE Clin Case Rep. 2025 Jan 6;11(2):138-142. doi: 10.1016/j.aace.2024.12.012. eCollection 2025 Mar-Apr.
BACKGROUND/OBJECTIVE: We present a case of a woman with persistent abdominal pain, leading to the discovery of a rare solitary fibrous tumor (SFT) in the adrenal gland. The rarity of adrenal SFTs and their diagnostic challenges make this case noteworthy. The objective of this report is to describe a patient with an adrenal SFT, highlighting the unique diagnostic approach and management considerations for this rare condition.
A 35-year-old woman presented with chronic abdominal pain and was referred to the endocrinology clinic for evaluation of an adrenal incidentaloma. Computed tomography imaging revealed a 4 cm homogeneous right adrenal mass, with precontrast Hounsfield units of 1 and an absolute contrast washout of 60%. A prior computed tomography scan from 6 years earlier showed a 1.5 cm adenoma with similar characteristics. Despite normal hormonal levels, the tumor's growth and the patient's symptoms prompted surgical referral. The patient underwent robotic-assisted laparoscopic right adrenalectomy. Pathological examination identified a well-circumscribed SFT, measuring 3.7 × 3.6 × 2.9 cm.
Adrenal SFTs are rare, typically hormonally inactive, well-circumscribed masses that often present with abdominal pain. While more common in the pleura, adrenal SFTs can mimic other benign adrenal lesions on imaging, complicating diagnosis. Histopathology is essential for accurate diagnosis, and surgical resection remains the main treatment.
This case highlights the diagnostic challenges of adrenal SFTs, which can mimic other benign lesions. Despite significant growth, the tumor was histologically benign with low malignancy risk. Clinicians should consider adrenal SFTs in the differential diagnosis of incidental adrenal masses with atypical imaging features.
背景/目的:我们报告一例患有持续性腹痛的女性病例,该病例导致在肾上腺发现了一种罕见的孤立性纤维瘤(SFT)。肾上腺SFT的罕见性及其诊断挑战使得该病例值得关注。本报告的目的是描述一名患有肾上腺SFT的患者,突出这种罕见病症独特的诊断方法和管理考量。
一名35岁女性因慢性腹痛就诊,并被转诊至内分泌科门诊评估肾上腺偶发瘤。计算机断层扫描成像显示右侧肾上腺有一个4厘米的均匀肿块,平扫时Hounsfield单位为1,绝对对比剂洗脱率为60%。6年前的一次计算机断层扫描显示有一个1.5厘米的腺瘤,具有相似特征。尽管激素水平正常,但肿瘤的生长和患者的症状促使其接受手术转诊。患者接受了机器人辅助腹腔镜右肾上腺切除术。病理检查确定为一个边界清晰的SFT,大小为3.7×3.6×2.9厘米。
肾上腺SFT很罕见,通常无激素活性,是边界清晰的肿块,常表现为腹痛。虽然在胸膜中更常见,但肾上腺SFT在影像学上可模仿其他良性肾上腺病变,使诊断复杂化。组织病理学对于准确诊断至关重要,手术切除仍然是主要治疗方法。
本病例突出了肾上腺SFT的诊断挑战,其可模仿其他良性病变。尽管肿瘤有显著生长,但在组织学上为良性,恶性风险低。临床医生在鉴别具有非典型影像学特征的肾上腺偶发肿块时应考虑肾上腺SFT。