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RESIDENT CASE STUDIES

October 16, 2003: Case 1 

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48 year old female with punch biopsy. Clinical history not provided.

Discussion by Michael Idowu, MD, and Farrukh H. Azmi, MD, PhD

Nodular melanosis is the term given to regressed melanoma with the presence of numerous melanophages. Partial regression of melanoma is seen in up to one third of melanomas.

Gross Appearance: Pigmented/depigmented macular lesions which may be previously pigmented and nodular. It may be seen in about 2% of patients with melanoma presenting with metastatic disease in the absence of recognized primary tumor.

Microscopic Appearance

  • There is presence of heavy lymphocytic infiltrate in the dermis with loss or degeneration of the tumor cells.
  • There are numerous melanophages.
  • Vascular fibrous tissue may be present.
  • It is noteworthy to know that there may not be melanophages in regressed melanoma, but their presence is necessary for the regression to be called "nodular melanosis. 

The initial punch biopsy in this case showed only abundant dermal melanophages with dermal lymphocytic infiltrate. This pattern should always make you suspicious of regressed melanoma and you should request a re-excision.

The re-excision however showed some residual melanocytic cells admixed with the lymphoid infiltrate. Since the malanophages may obscure the tumor cells, it may be necessary to bleach them. 

  • The residual tumor cells in the re-excision are positive for S100. 

It is important to know that this pattern of regression is not specific for nodular melanosis, it can be produced by solar lentigo and epithelial lesions such as basal cell carcinoma. S100 stain mat help in differentiating these from nodular melanosis.

Diagnostic Criteria

  • Abundant dermal melanophages
  • Abundant dermal lymphocytic infiltrate
  • Few residual tumor cells positive for S100

Immunostains:

  • S100

Differential Diagnosis:

  • Solar lentigo
  • Basal cell carcinoma
  • Pigment incontinence
  • Insect bite
  • Nevus

References:

  1. David Weedon: Skin Pathology. Churchill Livingstone 2002.