Post-traumatic Arthrofibrosis of the Knee Joint in a Patient with Familial Cutaneous Collagenoma and Recent ACL reconstruction with Hamstring Allograf

N. Carayannopoulos
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Abstract

Familial cutaneous collagenoma is a rare, autosomal dominant hereditary disease. These collagenous bundles are typically seen as hypopigmented, superficial skin lesions along the trunk and the upper limbs. We report a case in which a 31-year-old patient presented with a disproportionate growth of scar tissue in the knee joint after having almost non-existent flexion and continued pain for 3 months after ACL reconstruction despite aggressive rehabilitation with formal therapy. In this case, there was no organic cause of tissue overgrowth or reason to expect such a drastic change in the joint space so soon after surgery. Histopathology of tissue from the left knee showed dense fibroconnective tissue with myxoid change and granulation tissue. The overgrowth was diagnosed as a form of collagen disorder with increased amounts of irregularly arranged dense fascicular bundles of collagen which are similarly seen in familial cutaneous collagenoma. To the best of our knowledge, our case is the first reported case of post-traumatic arthrofibrosis in a patient with familial cutaneous collagenoma (FCC) in American literature.
家族性皮肤胶原瘤患者创伤后膝关节关节纤维化及近期同种异体腿筋重建前交叉韧带
家族性皮肤胶原瘤是一种罕见的常染色体显性遗传病。这些胶原束通常表现为沿躯干和上肢的低色素、浅表性皮肤病变。我们报告了一例31岁的患者,在ACL重建后几乎不存在屈曲和持续疼痛3个月后,膝关节瘢痕组织不成比例地生长,尽管经过了积极的康复治疗。在本例中,没有组织过度生长的器质性原因,也没有理由预期手术后关节间隙会发生如此剧烈的变化。左膝组织病理示致密纤维结缔组织伴黏液样改变及肉芽组织。过度生长被诊断为胶原蛋白紊乱的一种形式,胶原蛋白不规则排列的密集束状束数量增加,与家族性皮肤胶原瘤相似。据我们所知,本病例是美国文献中首次报道的家族性皮肤胶原瘤(FCC)患者创伤后关节纤维化的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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