Department of Pathology, North Hospital, University Hospital of St-Etienne, France; Department of Pathology, Facutly of Medicine, Jazan University, Jazan, Saudi Arabia.
Department of Pathology, North Hospital, University Hospital of St-Etienne, France.
Pathol Res Pract. 2020 Apr;216(4):152865. doi: 10.1016/j.prp.2020.152865. Epub 2020 Feb 12.
Granular cell tumor (GCT) remains a diagnostic clinicopathologic problem because the exact frequency of its detailed morphological and clinical characteristics is unknown as most observations are collected from small series or isolated cases. Herein, our aim is to highlight the frequency of all clinicopathological characteristics of this rare tumor based in our series and the available medical (PubMed) literature.
42 cases were evaluated for: tissue layers involved by the tumor (in skin and mucosae), growth pattern, nuclear pleomorphism, mitotic index, necrosis, spindling, calcification, hyalinization, and pustule-ovoid bodies of Milian, as well as perineural and vascular invasion, and the presence of adjacent epithelium changes, and lymphocytes and eosinophils infiltration., Follow-up was analyzed. The tumors were subclassified into benign, atypical and malignant according to Fanburg-Smith criteria and into benign or GCT of uncertain malignant potential according to Nasser criteria. The same characteristics were analyzed for 1499 cases reviewed according to PRISMA guidelines.
In the current series, the mean age at diagnosis was 45.8 years (range 6-69 years). Most patients were females (60 %) and the involved organs were by descending frequency: skin and subcutaneous tissue, bronchus, esophagus, breast, tongue, larynx, pharynx, gingiva, trachea, right colon, vulva, and hypopharynx. No recurrence or progression was seen, despite 32 cases were incompletely excised, with the exception of one malignant tumor. The growth pattern was either infiltrative (85.71 %) or well limited (7.14 %). Sixteen tumors had vesicular nuclei. Mitotic activity was found in two tumors. Lymphocytic infiltration was found in 14 tumors. Eosinophils were present in 6 cases. One GCT of the right colon showed extensive calcification and hyalinization. Perineural invasion was noted in 6 lesions. No vascular invasion was found. One tumor was clinically malignant and the patient died 2 years after diagnosis. Medical literature review showed similar results in terms of frequency of the reported clinical and morphological features. Among cases with available follow up, almost 20 % showed positive margins and of those 20 % developed local recurrence. According to the Fanburg-Smith criteria, 72 % would be benign, 17 % atypical and 11 % malignant tumors, while according to those of Nasser, 93 % would be benign and 7% of uncertain malignant potential. However, true malignancy, as affirmed by metastasis of GCT is found in almost 2.5 % of the cases.
GCT is a usually benign tumor, affecting any anatomic location. Necrosis and mitotic activity seem to be the most effective histologic criteria for detecting aggressive tumors, but the presence of metastasis (2.5 % of the cases) remains the most accepted definitive criterion for diagnosis of malignant GCT.
颗粒细胞瘤(GCT)仍然是一个诊断临床病理问题,因为其详细的形态和临床特征的确切频率尚不清楚,因为大多数观察结果都是从小样本或孤立病例中收集的。在此,我们旨在根据我们的系列和可用的医学(PubMed)文献,强调这种罕见肿瘤所有临床病理特征的频率。
评估了 42 例病例:肿瘤累及的组织层(皮肤和黏膜)、生长模式、核异型性、有丝分裂指数、坏死、梭形化、钙化、玻璃样变和米利安的脓疱-卵形体,以及神经周围和血管侵犯,以及邻近上皮变化、淋巴细胞和嗜酸性粒细胞浸润。分析了随访情况。根据 Fanburg-Smith 标准将肿瘤分为良性、非典型和恶性,根据 Nasser 标准将肿瘤分为良性或颗粒细胞瘤恶性潜能不确定。根据 PRISMA 指南对 1499 例病例进行了相同特征的分析。
在当前系列中,诊断时的平均年龄为 45.8 岁(范围 6-69 岁)。大多数患者为女性(60%),受累器官依次为:皮肤和皮下组织、支气管、食管、乳房、舌、喉、咽、牙龈、气管、右结肠、外阴和下咽。尽管 32 例病例未完全切除,但除 1 例恶性肿瘤外,未见复发或进展。生长模式为浸润性(85.71%)或局限性好(7.14%)。16 个肿瘤有泡状核。两个肿瘤中有有丝分裂活动。14 例肿瘤有淋巴细胞浸润。6 例有嗜酸性粒细胞。右结肠的一个 GCT 显示广泛的钙化和玻璃样变。6 例有神经周围侵犯。无血管侵犯。1 例肿瘤临床恶性,患者诊断后 2 年死亡。文献复习显示,在报告的临床和形态特征频率方面,结果相似。在有随访的病例中,近 20%的病例切缘阳性,其中 20%的病例局部复发。根据 Fanburg-Smith 标准,72%为良性,17%为非典型,11%为恶性肿瘤,而根据 Nasser 的标准,93%为良性,7%为恶性潜能不确定。然而,GCT 的转移所证实的真正恶性,在几乎 2.5%的病例中发现。
GCT 通常是一种良性肿瘤,可影响任何解剖部位。坏死和有丝分裂活动似乎是检测侵袭性肿瘤最有效的组织学标准,但转移(病例的 2.5%)仍然是诊断恶性 GCT 的最可接受的明确标准。