Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 59005, USA.
Department of Pathology, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA.
Virchows Arch. 2022 Nov;481(5):739-750. doi: 10.1007/s00428-022-03408-2. Epub 2022 Sep 7.
Plexiform fibrohistiocytic tumor (PFHT) is a mesenchymal tumor of intermediate malignancy, typically occurring in the superficial soft tissues of young patients and displaying a biphasic pattern, with nodules of histiocytoid cells surrounded by fascicles of myofibroblastic spindled cells. The pathogenesis of PHFT is unknown. We comprehensively studied 39 PFHT, occurring in 25 females (66%) and 13 males (34%), ranging from 2 to 55 years of age (median 21 years). The tumors most often occurred in the upper extremity (n = 16, 41%) and ranged from 0.4 to 6.1 cm in size (median 1.5 cm). One patient with known neurofibromatosis type 1 presented with metachronous tumors of the finger and back. Clinical follow-up (29 patients; range 5-168 months; median 60 months) showed 3 tumors to have recurred locally; none was metastasized. One patient died of an unrelated cause; all others were alive without disease at the time of last follow-up. Immunohistochemistry showed the histiocytoid nodules of all cases to contain CD163/CD11c-positive histiocytes and cells negative for both markers ("null cells"). CSF1 expression was present in "null cells" in 7/10 cases (RNAscope chromogenic in situ hybridization). The Ki-67 labeling index was very low (< 5%); Ki-67-positive cells within histiocytoid nodules appeared to represent "null cells." All tested cases were negative for significant mutations or fusion events (TruSight Mutation Panel, TruSight Fusion Panel, Mayo Clinic Melanoma Targeted Gene Panel). We conclude that PHFT may be even more indolent than has been appreciated, although classification as an "intermediate" tumor is correct. We hypothesize that the CSF1-producing "null cells" of PHFT may represent the neoplastic element, with the bulk of the tumor masses comprising recruited and reactive cell populations.
丛状纤维组织细胞瘤(PFHT)是一种中等恶性的间叶性肿瘤,通常发生在年轻患者的表浅软组织中,表现为双相模式,由组织细胞样细胞结节和梭形肌纤维母细胞束组成。PFHT 的发病机制尚不清楚。我们全面研究了 39 例 PFHT,其中 25 例为女性(66%),13 例为男性(34%),年龄 2 至 55 岁(中位年龄 21 岁)。肿瘤最常发生在上肢(n=16,41%),大小 0.4 至 6.1cm(中位 1.5cm)。1 例已知患有 1 型神经纤维瘤病的患者表现为手指和背部的同时性肿瘤。临床随访(29 例患者;范围 5-168 个月;中位 60 个月)显示 3 例肿瘤局部复发;无转移。1 例患者死于无关原因;所有其他患者在最后一次随访时均存活且无疾病。免疫组化显示所有病例的组织细胞样结节均含有 CD163/CD11c 阳性组织细胞和两种标志物均阴性的细胞(“空泡细胞”)。7/10 例(RNAscope 显色原位杂交)中存在 CSF1 在“空泡细胞”中的表达。Ki-67 标记指数非常低(<5%);组织细胞样结节内的 Ki-67 阳性细胞似乎代表“空泡细胞”。所有检测病例均未发现显著突变或融合事件(TruSight 突变面板、TruSight 融合面板、Mayo 诊所黑色素瘤靶向基因面板)。我们得出结论,PFHT 可能比以前认为的更惰性,尽管将其归类为“中间”肿瘤是正确的。我们假设 PFHT 中产生 CSF1 的“空泡细胞”可能代表肿瘤成分,肿瘤肿块的大部分由募集的和反应性细胞群体组成。