Cutaneous follicle center lymphoma
ICD-10 C82.6 is a billable code used to indicate a diagnosis of cutaneous follicle center lymphoma.
Cutaneous follicle center lymphoma (CFCL) is a type of non-Hodgkin lymphoma that primarily affects the skin. It is characterized by the proliferation of B-cells in the follicle center, leading to the formation of nodules or plaques on the skin. CFCL is considered a low-grade lymphoma, often presenting with indolent symptoms. Patients may experience localized skin lesions, which can be mistaken for other dermatological conditions. The disease is typically diagnosed through skin biopsy, where histological examination reveals neoplastic follicle center cells. Staging of CFCL is crucial, as it can influence treatment decisions. The Ann Arbor staging system is commonly used, which assesses the extent of disease involvement in the skin and lymph nodes. B-symptoms, such as fever, night sweats, and weight loss, may be present but are less common in CFCL compared to other lymphomas. Treatment options vary based on disease stage and may include topical therapies, radiation, and systemic therapies such as chemotherapy or immunotherapy. The prognosis for patients with CFCL is generally favorable, especially when diagnosed early and treated appropriately.
Detailed clinical notes on staging, treatment response, and follow-up care.
Diagnosis and management of CFCL, treatment planning, and monitoring for recurrence.
Ensure accurate staging and documentation of any B-symptoms to guide treatment.
Comprehensive skin examination notes, biopsy results, and treatment plans.
Evaluation of skin lesions, biopsy for diagnosis, and management of skin-related symptoms.
Differentiating CFCL from other dermatological conditions is crucial for accurate coding.
Used when a biopsy is performed to confirm CFCL diagnosis.
Pathology report must be included in the patient's medical record.
Ensure the pathology report clearly indicates the diagnosis of CFCL.
Common symptoms include solitary or multiple skin lesions, which may be nodular or plaque-like. Some patients may experience mild itching or discomfort, but systemic symptoms like fever and weight loss are less common.
