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骨化性化脓性肉芽肿:一种罕见的变异型,通常不易识别。

Ossifying pyogenic granuloma: A rare variant usually not recognized.

机构信息

Department of Pathology, Robert J. Tomsich Pathology and Laboratory Medicine, Cleveland Clinic, Ohio, USA.

出版信息

J Cutan Pathol. 2021 Jul;48(7):954-957. doi: 10.1111/cup.14007. Epub 2021 Mar 25.

Abstract

Pyogenic granuloma (PG) represents a polypoid and lobular, capillary lesion, resembling granulation tissue, usually occurring on skin or mucosal surfaces. The occurrence of metaplastic ossification is extremely rare in PG. We present three cases of PG with metaplastic ossification. All three patients were men, aged 18-66 years. In all cases, the lesions occurred on the digits, particularly in or around the nail bed. Histopathologically, these superficial dermal-based tumors were characterized by classic features of PG, namely circumscribed, exophytic to polypoid proliferations of capillary-sized blood vessels in a lobular arrangement. The characteristic vascular component also was intimately associated with spicules and trabeculae of metaplastic bone formation rimmed by osteoblasts and osteoclasts. This osseous component was diffusely distributed in two cases and more localized in another. We speculate that ossification in PGs possibly represents a reactive process in response to chronic injury. We believe that ossifying PG is likely under-recognized and often mistaken for other entities also arising in the extremities and characterized by osseous metaplasia.

摘要

化脓性肉芽肿(PG)表现为息肉样和小叶状、毛细血管病变,类似于肉芽组织,通常发生在皮肤或黏膜表面。PG 中发生化生性骨化极为罕见。我们报告了三例伴有化生性骨化的 PG。所有三例患者均为男性,年龄 18-66 岁。所有病例的病变均发生在手指上,特别是在甲床内或周围。组织病理学上,这些位于真皮浅层的肿瘤具有典型的 PG 特征,即边界清楚的、小叶状排列的毛细血管大小的血管外生性至息肉样增生。特征性的血管成分也与被成骨细胞和破骨细胞环绕的化生骨形成的刺和小梁密切相关。在两种情况下,这种骨成分呈弥漫性分布,另一种则更局限。我们推测 PG 中的骨化可能代表对慢性损伤的反应性过程。我们认为,发生骨化的 PG 可能被低估了,并且经常被误诊为其他也发生在四肢并伴有骨化性化生的病变。

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