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Reconstruction with free jejunal flap in dystrophic epidermolysis bullosa complicated with hypopharyngeal cancer: A case report.
Matsumoto, Daiki; Otani, Naoya; Seike, Shien; Kubo, Tateki.
Afiliação
  • Matsumoto D; Department of Plastic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Otani N; Department of Plastic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Seike S; Department of Plastic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Kubo T; Department of Plastic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Microsurgery ; 44(5): e31207, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38895936
ABSTRACT
Epidermolysis bullosa (EB) encompasses a range of rare genetic dermatological conditions characterized by mucocutaneous fragility and a predisposition to blister formation, often triggered by minimal trauma. Blisters in the pharynx and esophagus are well-documented, particularly in dystrophic EB (DEB). However, there have been few reports of mucocutaneous squamous cell carcinoma (SCC) in the head and neck region, for which surgery is usually avoided. This report presents the first case of free jejunal flap reconstruction after total pharyngolaryngoesophagectomy for hypopharyngeal cancer in a 57-year-old patient with DEB. The patient with a known diagnosis of DEB had a history of SCC of the left hand and esophageal dilatation for esophageal stricture. PET-CT imaging during examination of systemic metastases associated with the left-hand SCC revealed abnormal accumulation in the hypopharynx, which was confirmed as SCC by biopsy. Total pharyngolaryngoesophagectomy was performed, followed by reconstruction of the defect using a free jejunal flap. A segment of the jejunum, approximately 15 cm in length, was transplanted with multiple vascular pedicles. The patient made an uneventful recovery postoperatively and was able to continue oral intake 15 months later with no complications and no recurrence of SCC in the head and neck region. While cutaneous SCC is common in DEB, extracutaneous SCC is relatively rare. In most previous cases, non-surgical approaches with radiotherapy and chemotherapy were chosen due to skin fragility and multimorbidity. In the present case, vascular fragility and mucosal damage of the intestinal tract were not observed, and routine vascular and enteric anastomoses could be performed, with an uneventful postoperative course. Our findings suggest that highly invasive surgery, including free tissue transplantation such as with a free jejunal flap, can be performed in patients with DEB.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Neoplasias Hipofaríngeas / Epidermólise Bolhosa Distrófica / Procedimentos de Cirurgia Plástica / Retalhos de Tecido Biológico / Jejuno Limite: Humans / Male / Middle aged Idioma: En Revista: Microsurgery Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Neoplasias Hipofaríngeas / Epidermólise Bolhosa Distrófica / Procedimentos de Cirurgia Plástica / Retalhos de Tecido Biológico / Jejuno Limite: Humans / Male / Middle aged Idioma: En Revista: Microsurgery Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão