Retiform hemangioendothelioma in the infratemporal fossa and buccal area: a case report and literature review
2
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
We report a case of retiform hemangioendothelioma (RH) located in the infratemporal fossa and buccal area in a 13-year-old Korean boy. The tumor originated from the sphenoid bone of the infratemporal fossa area and spread into the cavernous sinus, orbital apex, and retro-nasal area with bone destruction of the pterygoid process. Tumor resection was conducted via Le Fort I osteotomy and partial maxillectomy to approach the infratemporal fossa and retro-nasal area. The diagnosis of RH was confirmed after surgery. In the presented patient, surgical excision was incomplete, and close follow-up was performed. There was no evidence of expansion or metastasis of the residual tumor in the 8 years after surgery. In cases of residual RH with low likelihood of expansion and metastasis, even though RH is an intermediate malignancy, close follow-up can be the appropriate treatment choice over additional aggressive therapy. To date, 29 papers and 48 RH cases have been reported, including this case. This case is the second reported RH case presenting as primary bone tumor and the first case originating in the oromaxillofacial area.
Abstract
We report a case of retiform hemangioendothelioma (RH) located in the infratemporal fossa and buccal area in a 13-year-old Korean boy. The tumor originated from the sphenoid bone of the infratemporal fossa area and spread into the cavernous sinus, orbital apex, and retro-nasal area with bone destruction of the pterygoid process. Tumor resection was conducted via Le Fort I osteotomy and partial maxillectomy to approach the infratemporal fossa and retro-nasal area. The diagnosis of RH was confirmed after surgery. In the presented patient, surgical excision was incomplete, and close follow-up was performed. There was no evidence of expansion or metastasis of the residual tumor in the 8 years after surgery. In cases of residual RH with low likelihood of expansion and metastasis, even though RH is an intermediate malignancy, close follow-up can be the appropriate treatment choice over additional aggressive therapy. To date, 29 papers and 48 RH cases have been reported, including this case. This case is the second reported RH case presenting as primary bone tumor and the first case originating in the oromaxillofacial area.
참고문헌 (31)
- Calonje E, "Retiform hemangioendothelioma. A distinctive form of low-grade angiosarcoma delineated in a series of 15 cases", Am J Surg Pathol, 18, pp.115~125 (1994)
- Fukunaga M, "Ushigome S. Retiform haemangioendothelioma", Virchows Arch, 428, pp.301~304 (1996)
- Aditya GS, "Epithelioid and retiform hemangioendothelioma of the skull bone--report of four cases", Indian J Pathol Microbiol, 46, pp.645~649 (2003)
- El Darouti M, "Retiform hemangioendothelioma", Int J Dermatol, 39, pp.365~368 (2000)
- Tan D, "Retiform hemangioendothelioma:a case report and review of the literature", J Cutan Pathol, 32, pp.634~637 (2005)
- Serel S, "Congenital retiform hemangioendothelioma", Indian J Dermatol, 52, pp.160~162 (2007)
- O'Duffy F, "A rare angiosarcoma: retiform haemangioendothelioma", J Laryngol Otol, 126, pp.200~202 (2012)
- Albertini AF, "Retiform hemangioendothelioma developed on the site of an earlier cystic lymphangioma in a six-year-old girl", Am J Dermatopathol, 33, pp.e84~87 (2011)
- Zhang G, "A case of retiform-hemangioendothelioma with unusual presentation and aggressive clinical features", Int J Clin Exp Pathol, 3, pp.528~533 (2010)
- Hirsh AZ, "Unresectable retiform hemangioendothelioma treated with external beam radiation therapy and chemotherapy: a case report and review of the literature", Sarcoma (2010)[DOI]
- Duke D, "Multiple retiform hemangioendotheliomas. A low-grade angiosarcoma", Am J Dermatopathol, 18, pp.606~610 (1996)
- Dufau JP, "Retiform hemangioendothelioma", Ann Pathol, 17, pp.47~51 (1997)
- Mentzel T, "Retiform hemangioendothelioma. Clinico-pathologic case report and discussion of the group of low malignancy vascular tumors", Pathologe, 18, pp.390~394 (1997)
- Sanz-Trelles A, "Retiform hemangioendothelioma. A new case in a child with diffuse endovascular papillary endothelial proliferation", J Cutan Pathol, 24, pp.440~444 (1997)
- Schommer M, "Retiform hemangioendothelioma: another tumor associated with human herpesvirus type 8?", J Am Acad Dermatol, 42, pp.290~292 (2000)
- Ulrich D, "Fast growing multifocal retiform hemangioendothelioma:a case report", Eur J Plast Surg, 25, pp.47~49 (2002)
- Coutinho MLF, "Laser indications hemangiomas in children", An Acad Nac Med, 162, pp.74~76 (2002)
- Escudero AG, "Retiform hemangioendothelioma: a report of two cases and literature review", Acta Dermosifiliogr, 94, pp.102~106 (2003)
- Botros MF, "Retiform hemangioendothelioma", Egypt Dermatol Online J, 1, pp.1~4 (2005)
- Ioannidou D, "Retiform hemangioendothelioma presenting as bruiselike plaque in an adult woman", Int J Dermatol, 45, pp.53~55 (2006)
- Parsons A, "Retiform hemangioendotheliomas usually do not express D2-40 and VEGFR-3", Am J Dermatopathol, 30, pp.31~33 (2008)
- Love WE, "Surgical management of congenital dermatofibrosarcoma protuberans", J Am Acad Dermatol, 61, pp.1014~1023 (2009)
- Bhutoria B, "Retiform hemangioendothelioma with lymph node metastasis: a rare entity", Indian J Dermatol Venereol Leprol, 75, pp.60~62 (2009)
- Emberger M, "Retiform hemangioendothelioma:presentation of a case expressing D2-40", J Cutan Pathol, 36, pp.987~990 (2009)
- Kajo K, "Retiform hemangioendotelioma in a 8-year-old girl--case report", Cesk Patol, 45, pp.72~74 (2009)
- Aydingöz IE, "Correspondence: retiform hemangioendothelioma presenting as a hyperhidrotic tumor", Int J Dermatol, 49, pp.1076~1077 (2010)
- Woo Kyung Choi, "Retiform Hemangioendothelioma on the Finger", Archives of Plastic Surgery, 39(1), pp.80~82 (2012), 대한성형외과학회
- Findikçioğlu K, "Retiform hemangioendothelioma originated from capillary malformation: a rare case", Turk J Plast Surg, 20, pp.12~15 (2012)
- Requena L, "Hemangioendothelioma", Semin Diagn Pathol, 30, pp.29~44 (2013)
- Zhang M, "Update on the infratemporal fossa approaches to nasopharyngeal angiofibroma", Laryngoscope, 108, pp.1717~1723 (1998)
- Roche PH, "Surgical anatomy of the infratemporal fossa using the transmaxillary approach", Surg Radiol Anat, 23, pp.209~213 (2001)