Shioya Yuta, Ando Hirofumi, Miyamoto Tsutomu, Ida Koichi, Kobara Hisanori, Yamaguchi Tomomi, Kosho Tomoki, Shiozawa Tanri
Department of Obstetrics and Gynecology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan.
Department of Medical Genetics, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan.
Gynecol Oncol Rep. 2024 Dec 31;57:101675. doi: 10.1016/j.gore.2024.101675. eCollection 2025 Feb.
Musculocontractural Ehlers-Danlos syndrome (mcEDS) is a rare autosomal recessive connective tissue disorder caused by systemic depletion of dermatan sulfate. Symptoms characteristic of mcEDS include multiple contractures, fragile skin with subcutaneous bleeding, and hypermobile joints, which suggest difficulty in perioperative management. However, safe surgical techniques and perioperative management of this disorder remain unknown because of its rarity. We report a patient with mcEDS who developed endometrial cancer and underwent surgery, with emphasis on perioperative management.
A female patient, who had been genetically diagnosed with mcEDS-CHST14 at the age of 25, presented with symptoms characteristic of mcEDS, including: congenital contractures of fingers and clubfeet, recurrent joint dislocation, progressive foot and spinal deformities, and large subcutaneous hematomas. At age 33, she had been diagnosed with atypical endometrial hyperplasia, and scheduled to undergo total abdominal hysterectomy. To address the risk of massive hemorrhage during the surgery due to mcEDS-related tissue fragility, plasma-derived factor VIII concentrate was prophylactically administered before surgery. During the surgery, neither fragility, hyperextensibility, nor hemorrhagic tendency of the uterus or adnexa observed was observed. The surgery was uneventful, with blood loss of 180 mL and operative time of 2 h and 54 min. However, on the sixth postoperative day, a 2.5-cm dissection was noted at the site of skin incision. Subcutaneous fluid accumulation developed under the skin incision and it persisted for 1.5 months. The postoperative pathological diagnosis was endometrioid carcinoma grade 1, stage IA.
The present case suggested that the prophylactic use of factor VIII was effective for the prevention of hemorrhage during surgery. However, delayed wound healing of the skin and subcutaneous tissues was considered a subject for future improvement.
肌肉挛缩型埃勒斯-当洛综合征(mcEDS)是一种罕见的常染色体隐性遗传性结缔组织疾病,由硫酸皮肤素系统性缺乏引起。mcEDS的特征性症状包括多处挛缩、伴有皮下出血的脆弱皮肤以及关节活动过度,这提示围手术期管理存在困难。然而,由于其罕见性,这种疾病的安全手术技术和围手术期管理仍不为人知。我们报告了一名患有mcEDS的患者,该患者罹患子宫内膜癌并接受了手术,重点介绍围手术期管理情况。
一名女性患者,25岁时经基因诊断为mcEDS-CHST14型,表现出mcEDS的特征性症状,包括:手指和马蹄足先天性挛缩、复发性关节脱位、足部和脊柱进行性畸形以及大量皮下血肿。33岁时,她被诊断为非典型子宫内膜增生,并计划接受全腹子宫切除术。为应对因mcEDS相关组织脆弱导致的手术中大量出血风险,术前预防性给予血浆源性凝血因子VIII浓缩物。手术过程中,未观察到子宫或附件有脆弱、过度伸展或出血倾向。手术顺利,失血180毫升,手术时间为2小时54分钟。然而,术后第六天,皮肤切口处发现一个2.5厘米的切口裂开。皮肤切口下出现皮下积液,并持续了1.5个月。术后病理诊断为1级子宫内膜样癌,IA期。
本病例表明,预防性使用凝血因子VIII对预防手术期间出血有效。然而,皮肤和皮下组织伤口愈合延迟被认为是未来需要改进的问题。