TY - JOUR
T1 - Resection and immediate reconstruction of two pediatric intraosseous capillary mandibular malformations
AU - Matsumoto, Hiroshi
AU - Ota, Tomoyuki
AU - Komagoe, Sho
AU - Noda, Yohei
AU - Makino, Takuma
AU - Takeda, Seiko
AU - Mizukawa, Nobuyoshi
AU - Taniguchi, Kohei
AU - Ikeda, Tomoka
AU - Yanai, Hiroyuki
AU - Kimata, Yoshihiro
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022
Y1 - 2022
N2 - Vascular anomalies arising in the mandible comprise under 1% of all intraosseous tumors originating from the mandible, and their occurrence is extremely rare. Few pediatric cases of mandibular capillary vascular malformations have been reported. We report two pediatric intraosseous capillary mandibular malformations with a similar clinical course. A 15-year-old boy and 10-year-old girl each developed a painless, rapidly growing mandibular swelling. Imaging and tissue biopsy did not establish a definitive diagnosis. As the destruction of the mandible progressed, mandibular resection and reconstruction were performed, and capillary malformation was diagnosed on the grounds of tissue examination. There has been no postoperative recurrence, and good function and appearance have been maintained. Mandibular vascular malformations require prompt, appropriate diagnosis and treatment because bone destruction progresses as the lesions grow. Although the surgical treatment of pediatric vascular malformations involves various problems peculiar to the growth phase, it is important to consider resection, including reconstruction, so that the postoperative function and appearance are not impaired. Level of evidence: Level V, therapeutic study.
AB - Vascular anomalies arising in the mandible comprise under 1% of all intraosseous tumors originating from the mandible, and their occurrence is extremely rare. Few pediatric cases of mandibular capillary vascular malformations have been reported. We report two pediatric intraosseous capillary mandibular malformations with a similar clinical course. A 15-year-old boy and 10-year-old girl each developed a painless, rapidly growing mandibular swelling. Imaging and tissue biopsy did not establish a definitive diagnosis. As the destruction of the mandible progressed, mandibular resection and reconstruction were performed, and capillary malformation was diagnosed on the grounds of tissue examination. There has been no postoperative recurrence, and good function and appearance have been maintained. Mandibular vascular malformations require prompt, appropriate diagnosis and treatment because bone destruction progresses as the lesions grow. Although the surgical treatment of pediatric vascular malformations involves various problems peculiar to the growth phase, it is important to consider resection, including reconstruction, so that the postoperative function and appearance are not impaired. Level of evidence: Level V, therapeutic study.
KW - Capillary malformation
KW - Intraosseous
KW - Mandible
KW - Pediatric
KW - Reconstruction
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U2 - 10.1007/s00238-021-01905-2
DO - 10.1007/s00238-021-01905-2
M3 - Article
AN - SCOPUS:85123252178
SN - 0930-343X
JO - European Journal of Plastic Surgery
JF - European Journal of Plastic Surgery
ER -