Perivascular Epithelioid Cell-Family Tumors in Children, Adolescents, and Young Adults: Clinicopathologic Features in 70 Cases.

Phoebe M Hammer, Angus Toland, Muhammad Shaheen, Archana Shenoy, Ashwini Esnakula, M John Hicks, Mikako Warran, Alyaa Al-Ibraheemi, Jessica L Davis, Serena Y Tan
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Abstract

Context.—: Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal tumors of uncertain histogenesis expressing smooth muscle and melanocytic markers. The clinicopathologic spectrum in young patients is not well documented.

Objective.—: To describe a multi-institutional series of PEComas in children, adolescents, and young adults.

Design.—: PEComas, not otherwise specified (NOS); angiomyolipomas (AMLs); lymphangioleiomyomatosis; and clear cell sugar tumors were retrospectively identified from 6 institutions and the authors' files.

Results.—: Seventy PEComas in 64 patients (median age, 15 years) were identified. They were more common in females (45 of 64 patients), occurring predominantly in the kidney (53 of 70), followed by the liver (6 of 70). Thirty-four patients had confirmed tuberous sclerosis complex (TSC), 3 suspected TSC mosaicism, 2 Li-Fraumeni syndrome (LFS) and 1 neurofibromatosis type 1. Most common variants were classic (49 of 70) and epithelioid (8 of 70) AML. Among patients with AMLs, most (34 of 47) had TSC, and more TSC patients had multiple AMLs (15 of 36) than non-TSC patients (2 of 13). Two TSC patients developed malignant transformation of classic AMLs: 1 angiosarcomatous and 1 malignant epithelioid. Lymphangioleiomyomatosis (5 of 70) occurred in females only, usually in the TSC context (4 of 5). PEComas-NOS (6 of 70) occurred exclusively in non-TSC patients, 2 of whom had LFS (2 of 6). Three were malignant, 1 had uncertain malignant potential, and 2 were benign. All 4 PEComas-NOS in non-LFS patients had TFE3 rearrangements.

Conclusions.—: Compared to the general population, TSC was more prevalent in our cohort; PEComas-NOS showed more frequent TFE3 rearrangements and possible association with LFS. This series expands the spectrum of PEComas in young patients and demonstrates molecular features and germline contexts that set them apart from older patients.

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儿童、青少年和年轻人中的血管周围上皮样细胞家族肿瘤:70 例病例的临床病理特征。
背景血管周围上皮样细胞瘤(PEComas)是一种罕见的间叶肿瘤,组织发生机制不明确,表达平滑肌和黑素细胞标记。其在年轻患者中的临床病理范围尚未得到很好的记录:描述儿童、青少年和年轻成人PEComas的多机构系列病例:从 6 家机构和作者的档案中回顾性地确定了未注明的 PEComas、血管肌脂肪瘤 (AML)、淋巴管瘤病和透明细胞糖瘤:64名患者(中位年龄15岁)中有70例PEC瘤。这些肿瘤多见于女性(64 例患者中有 45 例),主要发生在肾脏(70 例患者中有 53 例),其次是肝脏(70 例患者中有 6 例)。34例患者确诊为结节性硬化综合征(TSC),3例疑似TSC嵌合,2例为李-弗劳米尼综合征(LFS),1例为神经纤维瘤病1型。最常见的变异型是典型急性髓细胞性白血病(70 例中有 49 例)和上皮样白血病(70 例中有 8 例)。在患有急性髓细胞性白血病的患者中,大多数(47例中的34例)患有TSC,而患有多发性急性髓细胞性白血病的TSC患者(36例中的15例)多于非TSC患者(13例中的2例)。两名TSC患者发生了典型急性髓细胞性白血病的恶性转化:1例为血管肉瘤型,1例为恶性上皮样型。淋巴管瘤病(70例中的5例)仅发生在女性患者中,通常是在TSC背景下发生(5例中的4例)。PEComas-NOS(70 例中有 6 例)仅发生在非 TSC 患者中,其中 2 例有 LFS(6 例中有 2 例)。其中 3 例为恶性,1 例恶性可能性不确定,2 例为良性。非LFS患者的4例PEComas-NOS均有TFE3重排:结论:与普通人群相比,TSC在我们的队列中发病率更高;PEComas-NOS显示出更频繁的TFE3重排,并可能与LFS有关。该系列病例扩大了年轻患者PEComas的范围,并显示了有别于老年患者的分子特征和种系背景。
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