An osteolytic lesion of the proximal ulna in a patient with Maffucci syndrome: a case report
- Author:
Hyeon Jun KIM
1
;
Sung Yoon JUNG
;
Ji Woong KIM
;
Min Gyung PARK
Author Information
- Publication Type:Case Report
- From: Archives of hand and microsurgery 2024;29(3):173-178
- CountryRepublic of Korea
- Language:English
- Abstract: Maffucci syndrome is a rare, congenital, and nonhereditary syndrome characterized by the occurrence of multiple enchondromas and hemangiomas. According to previous studies, patients diagnosed with Maffucci syndrome have a higher risk of developing malignant tumors, such as ovarian cancer, pancreatic cancer, breast cancer, and central nervous system cancer, in addition to malignant transformations of enchondromas. The authors report a case of a 37-year-old male patient with Maffucci syndrome who presented with multiple enchondromas and hemangiomas. This patient’s presentation and management are discussed, along with a review of the literature. Maffucci syndrome should be expected when encountering a patient with multiple enchondromas and suspected hemangiomas in the limbs. Even if benign lesions such as enchondromas or hemangiomas are diagnosed, regular follow-up is required to monitor for malignant transformations and the development of malignant tumors in other organs.
