Regmi Aayushma, Raouf Maryam, Mudaliar Kumaran M, Speiser Jodi J, Ananthanarayanan Vijayalakshmi
Department of Pathology and Laboratory Medicine, Loyola University Medical Center, Maywood, IL; and.
Dallas Methodist Medical Center, Dallas, TX.
Am J Dermatopathol. 2023 Feb 1;45(2):127-132. doi: 10.1097/DAD.0000000000002348.
A 32-year-old G2P1L1 (5 months pregnant) woman presented with a 3-month history of a slow-growing cystic lesion on her scalp vertex. Similar lesions in the exact location were excised twice in the past with a diagnosis of trichilemmal carcinoma (TC). A biopsy of the scalp lesion showed morphology and immunoprofile consistent with previously diagnosed TC. Staging PET/CT demonstrated a 4.7 cm right upper lobe lung, and a subsequent lung biopsy showed a small, round blue-cell tumor with necrosis, morphologically identical to the prior biopsies from the scalp. Considering the unusual clinical course of TC, a lung biopsy was sent for next-generation sequencing that showed EWSR1-FLI1 (type1) fusion. Additionally, CD99 immunostaining revealed uniform cytoplasmic and membranous staining in the tumor cells. The previous scalp excision specimen was also sent for mutation analysis, which showed EWSR1-FLI1 fusion. In conjunction with clinical history and histological and molecular findings, a definitive diagnosis of primary cutaneous Ewing sarcoma (PCES) with local recurrence and metastasis to the lung was made. We present a case of PCES, which was previously misdiagnosed and treated as TC. This case emphasizes the importance of CD99 in the initial screening of cutaneous small round blue-cell tumors to avoid misdiagnosis from other morphological overlaps. Also, despite its rarity, PCES should be included in the differential diagnosis of small, round, blue cell tumors at cutaneous sites. Our case also exemplifies common biases in medical decision-making, including premature closure and anchoring bias which can result in misdiagnosis or diagnostic delay and associated delay in appropriate management.
一名32岁、孕2产1(妊娠5个月)的女性患者,头皮顶部有一个生长缓慢的囊性病变,病史3个月。过去曾在同一确切位置切除过类似病变,两次均诊断为毛母质癌(TC)。头皮病变活检显示形态学和免疫表型与先前诊断的TC一致。分期PET/CT显示右上肺叶有一个4.7 cm的病灶,随后的肺活检显示为一个小的圆形蓝细胞瘤伴坏死,形态学上与先前头皮活检结果相同。考虑到TC不寻常的临床病程,肺活检标本送去进行二代测序,结果显示EWSR1-FLI1(1型)融合。此外,CD99免疫染色显示肿瘤细胞胞质和细胞膜呈均匀染色。之前的头皮切除标本也送去进行突变分析,结果显示EWSR1-FLI1融合。结合临床病史、组织学和分子学检查结果,最终诊断为原发性皮肤尤文肉瘤(PCES)伴局部复发和肺转移。我们报告了一例曾被误诊为TC并接受相应治疗的PCES病例。该病例强调了CD99在皮肤小圆形蓝细胞瘤初步筛查中的重要性,以避免因形态学重叠而误诊。此外,尽管PCES罕见,但在皮肤部位小圆形蓝细胞瘤的鉴别诊断中应考虑到该病。我们的病例还例证了医疗决策中常见的偏差,包括过早下结论和锚定偏差,这些偏差可能导致误诊或诊断延迟以及相应的治疗延迟。