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Evaluation of the Role of Routine Melan-A Immunohistochemistry for Exclusion of Microinvasion in 120 Cases of Lentigo Maligna

Suchak, Ravi MBChB, MSc, DipRCPath*,†; Hameed, Omair Akhtar MBBS, BSc, MRCP*; Robson, Alistair MBChB, BSc (Hons), MRCPath, DipRCPath

American Journal of Dermatopathology: May 2014 - Volume 36 - Issue 5 - p 387–391
doi: 10.1097/DAD.0b013e3182a3877a
Original Study

Background: To assess the usefulness of routine melan-A immunohistochemistry (IHC) for exclusion of microinvasion in lentigo maligna (LM).

Methods: One hundred and twenty cases of LM from our archives were reviewed by 2 authors with S100 protein and melan-A IHC using a red chromogen.

Results: Melan-A was useful to confirm the diagnosis of LM in early lesions and to differentiate these from chronically sun-damaged skin. The presence of scattered melan-A–positive cells was noted in the dermis in 72 of 120 cases (melanophages in 36 cases, nonspecific cells different to melanophages in 16 cases, and a dual cell population in 20 cases). The significance of these cells was uncertain. Only 3 cases suspicious for microinvasion were identified: 2 on haematoxylin and eosin and 1 on S100.

Conclusions: We recommend use of melan-A to confirm the diagnosis in early lesions of LM and in the differential diagnosis from melanocytic hyperplasia in chronically sun-exposed skin. We do not recommend routine use of melan-A to identify or exclude microinvasion. However, it may have a role, in conjunction with S100, in cases with suspicious features for early invasion on haematoxylin and eosin sections.

*Department of Dermatology, Basildon University Hospital, Essex, United Kingdom; and

Department of Dermatopathology, St John's Institute of Dermatology, St Thomas' Hospital, London, United Kingdom.

Reprints: Omair Akhtar Hameed, MBBS, BSc, MRCP, Department of Dermatology, Basildon University Hospital, Nethermayne, Basildon, Essex SS165NL, United Kingdom (e-mail: omair.hameed@btuh.nhs.uk).

The authors declare no conflicts of interest.

Presented at the Dermatopathology Special Interest Group at the BAD Annual Meeting on July 3, 2012; Brimingham, UK.

© 2014 by Lippincott Williams & Wilkins.