Learn about Anterior Basement Membrane Dystrophy (ABMD), also known as Epithelial Basement Membrane Dystrophy, Map-Dot-Fingerprint Dystrophy, and Cogan's Microcystic Dystrophy. This page provides information on diagnosis, clinical documentation, and medical coding for ABMD, a common corneal dystrophy. Find resources for healthcare professionals, including ICD-10 codes and clinical findings related to Anterior Basement Membrane Dystrophy.
Also known as
Other specified corneal dystrophies
This code encompasses other specific corneal dystrophies, including anterior basement membrane dystrophy.
Other corneal dystrophies
This includes various corneal dystrophies not classified elsewhere.
Disorders of cornea
This category covers a wide range of corneal disorders, including dystrophies.
Follow this step-by-step guide to choose the correct ICD-10 code.
Is the diagnosis Anterior Basement Membrane Dystrophy or one of its synonyms?
Yes
Is there corneal scarring or neovascularization?
No
Do not code for Anterior Basement Membrane Dystrophy. Review clinical documentation for alternative diagnosis.
When to use each related code
Description |
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Inherited corneal dystrophy affecting the basement membrane. |
Corneal dystrophy causing recurrent erosions and pain. |
Corneal dystrophy featuring lattice-like lines in the stroma. |
Missing or incorrect laterality (right, left, bilateral) can impact reimbursement and data accuracy. ICD-10-CM requires specifying laterality for ABMD.
Coding to a less specific form of ABMD when clinical documentation supports a more specific subtype. This affects quality reporting and research.
Incorrectly using alternate names without cross-referencing to the primary diagnosis code for ABMD. This can lead to coding errors and data inconsistencies.
Q: What are the key clinical features differentiating Anterior Basement Membrane Dystrophy from other corneal dystrophies like Reis-Bucklers or macular dystrophy?
A: Anterior Basement Membrane Dystrophy (ABMD), also known as Epithelial Basement Membrane Dystrophy or Map-Dot-Fingerprint Dystrophy, can sometimes mimic other corneal dystrophies, particularly in early stages. However, key differentiating features can aid in diagnosis. Unlike Reis-Bucklers, which typically presents with recurrent painful erosions early in life and has a more central and diffuse haze, ABMD often exhibits a more peripheral and map-like, dot-like, or fingerprint-like pattern of corneal opacities. Compared to macular dystrophy, which involves stromal clouding and affects vision more significantly, ABMD primarily involves the epithelial basement membrane and superficial stroma, often causing minimal visual disturbance initially. Confocal microscopy can be invaluable in highlighting the characteristic findings of ABMD, such as thickening, duplication, and irregularities of the basement membrane, aiding in its differentiation from other corneal dystrophies. Consider implementing confocal microscopy as a diagnostic tool for confirming cases where the clinical presentation is ambiguous. Explore how different imaging modalities can further enhance your diagnostic accuracy in challenging cases.
Q: How should I manage recurrent corneal erosions in a patient with diagnosed Anterior Basement Membrane Dystrophy, and what are the latest evidence-based treatment options?
A: Recurrent corneal erosions are a common complication of Anterior Basement Membrane Dystrophy (ABMD), causing significant discomfort and impacting patient quality of life. Management should address both preventing erosions and promoting healing when they occur. Conservative approaches include lubricating eye drops, hypertonic saline ointment at night, and bandage contact lenses. For more persistent cases, anterior stromal puncture, phototherapeutic keratectomy (PTK), and diamond burr polishing can be considered. Recent studies have explored the use of amniotic membrane transplantation and cross-linking for refractory cases. Careful patient education on proper contact lens hygiene (if applicable) and avoiding eye rubbing is crucial. Explore the latest research on managing recurrent corneal erosions in ABMD to stay abreast of evolving best practices. Learn more about the pros and cons of different intervention strategies to tailor treatment to individual patient needs.
Anterior basement membrane dystrophy (ABMD), also known as epithelial basement membrane dystrophy, map-dot-fingerprint dystrophy, or Cogan's microcystic dystrophy, was diagnosed. The patient presented with complaints consistent with ABMD, including recurrent corneal erosions, blurred vision, foreign body sensation, and discomfort. Slit-lamp examination revealed characteristic findings of map-like, dot-like, and fingerprint-like corneal epithelial basement membrane changes. Corneal topography was performed to further assess the corneal surface irregularity. Patient history includes [Insert relevant patient ocular and medical history, including family history of corneal dystrophies, allergies, medications, and prior eye surgeries]. Differential diagnoses considered included other corneal dystrophies such as Reis-Bucklers dystrophy and Thiel-Behkens dystrophy, as well as recurrent corneal erosion syndrome. Based on the clinical presentation and examination findings, the diagnosis of anterior basement membrane dystrophy was established. The patient was educated about the nature of the condition, its typically slow progression, and the potential for recurrent episodes. Treatment options discussed included lubricating eye drops, hypertonic saline ointment, bandage contact lenses for pain relief, and epithelial debridement if indicated. The patient was advised on proper contact lens hygiene if applicable. Follow-up appointments were scheduled to monitor the disease progression and adjust the management plan as needed. ICD-10 code H18.51 (other specified corneal dystrophies) is appropriate for this diagnosis. This documentation supports medical necessity for the provided services and facilitates accurate medical billing and coding.