Department of Surgery, Department of Morphofunctional Sciences I, Grigore T. Popa University of Medicine and Pharmacy, Iaşi, Romania;
Rom J Morphol Embryol. 2021 Jan-Mar;62(1):233-238. doi: 10.47162/RJME.62.1.23.
Glomus tumors account for 1-4% of benign hand tumors. In 65% of cases, it is located in the nail bed. Its rarity makes misdiagnosis problems relatively common. Symptomatology is characterized by the hallmark symptomatic triad. Imaging investigations may guide the diagnosis, but the diagnosis is made by pathological examination doubled by immunohistochemical (IHC) markers.
PATIENTS, MATERIALS AND METHODS: We studied a group of seven female patients, aged 28 to 56 years. Clinical examination revealed the presence of the characteristic symptomatic triad. Ultrasound imaging tests were performed.
Anatomopathological examination made a diagnosis of glomus tumor in all seven cases. IHC staining showed that tumor cells were positive for alpha-smooth muscle actin (α-SMA) and h-caldesmon in all seven cases and negative for cluster of differentiation 34 (CD34) in 72.14%. IHC stainings for p63, S100, cytokeratin (CK) AE1∕AE3 were negative in all cases. The clinical diagnosis completed by ultrasonography was histopathologically confirmed in all cases.
Although the glomus tumor is a rare lesion, we need to be familiar with it because a diagnostic delay also implies a treatment delay which will lead to amplified suffering and even real disability due to the high-intensity pain in these cases.
血管球瘤占手部良性肿瘤的 1-4%。在 65%的病例中,它位于甲床。由于其罕见性,导致误诊问题较为常见。其症状表现为典型的三联征。影像学检查可指导诊断,但诊断需要病理检查和免疫组化(IHC)标志物双重证实。
患者、材料和方法:我们研究了一组 7 名女性患者,年龄 28 至 56 岁。临床检查显示存在特征性三联征。进行了超声影像学检查。
所有 7 例均经解剖病理学检查诊断为血管球瘤。IHC 染色显示,所有 7 例肿瘤细胞均α-平滑肌肌动蛋白(α-SMA)和 h-钙调蛋白阳性,CD34 阴性占 72.14%。所有病例的 p63、S100、细胞角蛋白(CK)AE1/AE3 的 IHC 染色均为阴性。所有病例均通过超声诊断完成临床诊断,并经组织病理学证实。
尽管血管球瘤是一种罕见的病变,但我们需要熟悉它,因为诊断延迟也意味着治疗延迟,这将导致这些病例的疼痛加剧,甚至真正的残疾,因为这些病例的疼痛强度很高。