Sonobe Yuta, Hasegawa Hiromasa, Hashimoto Kazuaki, Takamiya Hisatake, Yamawaki Yuka, Konishi Eiichi
Department of Surgical Pathology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Department of Laboratory Medicine, Diagnostic Pathology, Shinshu University Hospital, Nagano, Japan.
Pathol Int. 2025 Feb;75(2):100-104. doi: 10.1111/pin.13502. Epub 2024 Dec 13.
Tenosynovitis with psammomatous calcification (TPC) is an extremely rare condition. It was first described as a characteristic subtype of idiopathic calcifying tenosynovitis, with only 40 cases reported to date. Here, we present a case of TPC affecting a female patient in her late teens, with no relevant medical history. She presented with discomfort and pain in the right first toe. A 10-mm mushroom-like calcified mass was observed in the metatarsophalangeal joint on radiographs. The surgical specimen revealed chronic synovitis with calcification. Numerous psammomatous bodies are observed in the synovium, often with granulomatous reactions. After removal of the mass, no recurrence has been observed for 5 years. Although the etiology of TPC has been suggested to be related to repetitive trauma to the tendon or peritendinous soft tissue, the composition and mechanism of calcification remain unclear because of its rarity. In this report, we also discuss the calcification mechanism in TPC, supported by scanning electron microscopy and energy-dispersive x-ray spectroscopy findings.
伴有砂粒体样钙化的腱鞘炎(TPC)是一种极为罕见的病症。它最初被描述为特发性钙化性腱鞘炎的一种特征性亚型,迄今为止仅有40例报道。在此,我们报告一例TPC病例,患者为一名接近20岁的女性,无相关病史。她表现为右足第一趾不适和疼痛。X线片显示在跖趾关节处有一个10毫米的蘑菇状钙化肿块。手术标本显示为伴有钙化的慢性滑膜炎。在滑膜中观察到大量砂粒体,常伴有肉芽肿反应。肿块切除后,5年未见复发。尽管TPC的病因被认为与肌腱或肌腱周围软组织的反复创伤有关,但由于其罕见性,钙化的组成和机制仍不清楚。在本报告中,我们还结合扫描电子显微镜和能量色散X射线光谱分析结果讨论了TPC中的钙化机制。