Evidence map›Paper›PMID 41793483›Full record

ReviewOral and maxillofacial surgery2026

Excessive intraoperative hemorrhage during orthognathic surgery in a patient with neurofibromatosis type 1: a case report and literature review.

Nobuyuki Sasahara, Kazuyuki Yusa, Mao Nishikawa, Satoshi Kasuya, Masaru Satomi, Shigeo Ishikawa

Abstract readCase ReportsReview
In one paragraph

Review in Oral and maxillofacial surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Nobuyuki SasaharaDepartment of Dentistry, Oral and Maxillofacial Plastic and Reconstructive Surgery, Yamagata University Faculty of Medicine, 2-2-2 Iida-Nishi, Yamagata, 990-9585, Japan. nsasahara@med.id.yamagata-u.ac.jp.ORCID http://orcid.org/0009-0000-2673-9135
Kazuyuki YusaDepartment of Dentistry, Oral and Maxillofacial Plastic and Reconstructive Surgery, Yamagata University Faculty of Medicine, 2-2-2 Iida-Nishi, Yamagata, 990-9585, Japan.
Mao NishikawaDepartment of Dentistry and Oral Surgery, Yonezawa City Hospital, Yamagata, Japan.
Satoshi KasuyaDepartment of Dentistry and Oral Surgery, Okitama Public General Hospital, Yamagata, Japan.
Masaru SatomiSatomi Orthodontic Dentistry Clinic, Yamagata, Japan.
Shigeo IshikawaDepartment of Dentistry, Oral and Maxillofacial Plastic and Reconstructive Surgery, Yamagata University Faculty of Medicine, 2-2-2 Iida-Nishi, Yamagata, 990-9585, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeurofibromatosis type 1 (NF1) is an autosomal dominant disorder caused by NF1 gene mutations, resulting in neurofibromin deficiency and vascular fragility. Although excessive hemorrhage during surgery has been reported in patients with NF1, such complications during orthognathic surgery are extremely rare. CASE REPORT: A 26-year-old woman with NF1 presented with skeletal Class II malocclusion. Preoperative contrast-enhanced computed tomography and magnetic resonance imaging revealed no neurofibromas along the airway or near the surgical field. Le Fort I osteotomy and bilateral sagittal split ramus osteotomies were planned following orthodontic treatment. Considering the bleeding risk associated with NF1, 600 mL of autologous blood was collected preoperatively. During surgery, persistent diffuse microvascular bleeding occured without identifiable vessel injury. The total intraoperative estimated blood loss was 1,715 mL, approximately five times higher than the average value reported for combined Le Fort I osteotomy and bilateral sagittal split ramus osteotomies. Hemostasis was achieved using oxidized cellulose compression. The patient received autologous blood transfusion only and recovered without allogeneic transfusion. Postoperative hemoglobin improved gradually with oral iron therapy, and the patient was discharged on postoperative day 16 without further complications.

conclusionThis case highlights the potential for excessive hemorrhage during orthognathic surgery in a patient with NF1, even in the absence of apparent neurofibromas. Comprehensive preoperative vascular assessment and autologous blood preparation are essential. Surgeons should be prepared for prompt hemostatic management to ensure safe surgical outcomes in patients with NF1.

Indexed as

Blood Loss, SurgicalMalocclusion, Angle Class IINeurofibromatosis 1Orthognathic Surgical ProceduresAdultBlood Transfusion, AutologousCellulose, OxidizedFemaleHemostasis, SurgicalHumansMagnetic Resonance ImagingOsteotomy, Le FortOsteotomy, Sagittal Split RamusTomography, X-Ray ComputedCellulose, OxidizedAutologous bloodExcessive hemorrhageNeurofibromatosis type 1Orthognathic surgery

Identifiers

PMID41793483
PMCPMC12967438

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.