Maffucci Syndrome is a rare genetic disorder characterized by the development of multiple enchondromas, which are noncancerous tumors that form in the cartilage. These enchondromas primarily affect the bones of the hands and feet. Additionally, individuals with Maffucci Syndrome may also develop hemangiomas, which are abnormal blood vessels that form as benign growths on the skin or internal organs.
In the International Classification of Diseases, Tenth Revision (ICD-10), Maffucci Syndrome is classified under "Q78.8 - Other specified osteochondrodysplasias." This code is used to identify and categorize various types of skeletal disorders involving abnormal development of bones and cartilage. By assigning this code, healthcare professionals can accurately document and track the prevalence of Maffucci Syndrome cases.
As for the corresponding ICD-9 code, it is "756.59 - Other enchondromatosis." ICD-9 codes were used prior to the implementation of ICD-10 and provided a similar classification system for medical diagnoses. This code specifically encompasses various conditions characterized by multiple enchondromas, including Maffucci Syndrome.
It's important to note that ICD codes are crucial for medical billing, research, and statistical purposes. These codes facilitate accurate documentation of patients' conditions, ensuring effective communication among healthcare providers and researchers worldwide. However, it's essential to consult with a qualified healthcare professional to obtain an accurate diagnosis and appropriate treatment for any medical concerns, including Maffucci Syndrome.
Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2023-07-10
Medical disclaimer:
This information does not substitute professional medical advice. Always consult your doctor before making health decisions.