Multifocal and unisystemic Langerhans-cell histiocytosis digital illustration

Multifocal and unisystemic Langerhans-cell histiocytosis Save


ICD-10 code: C96.5

Chapter: Neoplasms

Multifocal and Unisystemic Langerhans-Cell Histiocytosis: Understanding the Difference

Langerhans-cell histiocytosis (LCH) is a rare disease that affects the body's immune system. It occurs when the Langerhans cells, a type of immune cell that helps the body fight off infections, start to grow and multiply abnormally. This can lead to the formation of tumors, damage to organs, and other serious health problems.

There are two types of LCH: multifocal and unisystemic. Here's what you need to know about the difference between them:

  1. Multifocal LCH: This type of LCH is more common in children and affects multiple parts of the body. The symptoms can vary depending on which organs are affected but may include bone pain, skin rashes, fever, and swollen lymph nodes. Treatment for multifocal LCH may include chemotherapy, radiation therapy, and other medications to help manage the symptoms.
  2. Unisystemic LCH: This type of LCH usually affects only one part of the body, such as the skin or bones. The symptoms may include skin lesions, bone pain, or other problems specific to the affected area. Treatment for unisystemic LCH may involve surgery to remove the affected tissue or medication to reduce inflammation.

It's important to note that LCH is a rare disease, and the symptoms can vary widely depending on the individual. If you or someone you know is experiencing symptoms of LCH, it's important to talk to a healthcare provider as soon as possible to get an accurate diagnosis and start treatment.

Overall, understanding the difference between multifocal and unisystemic LCH can help you better understand this rare disease and what to expect if you or someone you know is affected. With early diagnosis and proper treatment, many people with LCH are able to manage their symptoms and live full, healthy lives.

Diagnosis Codes for Multifocal and unisystemic Langerhans-cell histiocytosis | C96.5