M11.132
Familial chondrocalcinosis, left wrist
Clinical Classification Guidelines
Medical Intelligence & Overview
Familial chondrocalcinosis, also known as calcium pyrophosphate deposition disease (CPPD), is a condition characterized by the buildup of calcium pyrophosphate crystals in the cartilage of joints. When localized to the left wrist, it can cause pain, swelling, and stiffness in that specific area. This condition tends to run in families, indicating a hereditary component. Recognizing and understanding familial chondrocalcinosis is important for proper management and to differentiate it from other joint disorders.
Causes & Symptoms
Clinical Causes: Genetic predisposition that leads to abnormal cartilage metabolism Age-related changes increasing likelihood of crystal deposition Metabolic disorders such as hyperparathyroidism, hemochromatosis, or hypothyroidism Joint trauma or injury that may predispose to crystal formation Previous joint surgery or inflammation
Key Symptoms: Joint pain, especially during movement or pressure Swelling and warmth around the affected joint Stiffness, limiting range of motion in the wrist Possible redness and tenderness over the joint Gradual worsening of symptoms over time
Diagnostic & Treatment
Diagnosis Path: Diagnosing familial chondrocalcinosis involves a combination of physical examination, medical history review, and imaging. Key diagnostic tools include:
Treatment Protocols: While there is no cure for familial chondrocalcinosis, treatment aims to manage symptoms and improve joint function. Typical approaches include:
Clinical Advice & FAQs
Billing Guidance
Is M11.132 a billable ICD-10 code?
Yes, M11.132 is a specific, billable code that can be used to indicate a diagnosis for reimbursement purposes.
Documentation
How do I report M11.132?
Clinical documentation must specify the nature of Familial chondrocalcinosis, left wrist and any associated comorbidities for accurate reporting.
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