Nakazawa Risa, Dohi Teruyuki, Hatsuoka Yuichi, Kigure Ryuta, Ogawa Rei
Department of Plastic, Reconstructive and Aesthetic Surgery, Nippon Medical School, Tokyo, Japan.
JPRAS Open. 2022 Dec 1;35:24-28. doi: 10.1016/j.jpra.2022.11.005. eCollection 2023 Mar.
Fibroma of tendon sheath (FTS) is a rare soft tissue tumor that usually occurs in the upper extremity. Moreover, of the few cases reported in the feet, nearly all occur in the plantar region. We report the case of a large FTS in the dorsum of the left foot that grew quickly into a 4 cm-diameter lesion. The 44-year-old Japanese man noticed the tumor incidentally one year before presentation and could not recall any possible cause. Physical examination showed an elastic hard mass that spread over the third to fifth metatarsal bones. MRI showed iso-intense signals with central hypo-intensity on T1-weighted images and hypo-intense signals on T2-weighted images. Since a biopsy did not reveal any malignant findings, the lesion was excised surgically. The tumor was found to be multilocular, encapsulated, and to arise from the extensor digitorum brevis tendon. Histopathology showed scattered spindle fibroblasts and slit-like vascular structures within the dense collagenous matrix. The tumor was diagnosed on the basis of the clinical, demographic, surgical, and histopathological findings as an FTS arising from the extensor digitorum brevis tendon. A review of the literature revealed seven cases of FTS of the dorsum of the foot, which indicates its rarity. More than one-half of these cases were from Japan. While the cause of FTS remains unclear, trauma has been implicated. We suggest that the cultural background of the patient, which could promote kneeling-induced dorsal foot trauma, may have contributed to the onset/progression of our case. Level of Clinical Evidence: 4.
腱鞘纤维瘤(FTS)是一种罕见的软组织肿瘤,通常发生在上肢。此外,在足部报道的少数病例中,几乎所有病例都发生在足底区域。我们报告一例发生在左脚背的大型FTS,该肿瘤迅速生长为直径4厘米的病变。这位44岁的日本男性在就诊前一年偶然发现了该肿瘤,且回忆不起任何可能的病因。体格检查显示一个弹性硬肿块,蔓延至第三至第五跖骨。MRI显示在T1加权图像上为等信号,中央低信号,在T2加权图像上为低信号。由于活检未发现任何恶性病变,故对该病变进行了手术切除。发现肿瘤为多房性、有包膜,起源于趾短伸肌腱。组织病理学显示在致密的胶原基质内有散在的梭形成纤维细胞和裂隙状血管结构。根据临床、人口统计学、手术和组织病理学检查结果,该肿瘤被诊断为起源于趾短伸肌腱的FTS。文献回顾显示有7例足部背侧FTS病例,表明其罕见性。其中一半以上的病例来自日本。虽然FTS的病因尚不清楚,但创伤被认为与之有关。我们认为患者的文化背景可能会增加因跪姿导致的足背创伤,这可能是导致我们这个病例发病/进展的原因。临床证据水平:4级。