Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 2005-2009  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Publishing Ltd/Inc.
    Journal of cutaneous pathology 32 (2005), S. 0 
    ISSN: 1600-0560
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: We describe here the case of a female patient with an otherwise classic invasive melanoma of the upper extremity, demonstrating the typical immunohistochemical profile, who presented three years later with massive ipsilateral axillary node metastases. The metastatic tumor had morphologic features similar to the primary melanoma, however at immunohistochemical level the tumor cells not only gained expression of pan-cytokeratin (AE1/AE3) but also lost expression of all standard melanoma markers (S100, Melan-A, HMB-45, MIT-1, and tyrosinase) thus mimicking a poorly differentiated mammary carcinoma. Additional stains reveal expression of Vimentin, NSE, c-kit, CD10 and negativity for CK7, CK20, BR2, ER/PR, mucin, and LCA. To rule out a breast carcinoma, real-time RT-PCR was performed on a lymph node using six breast cancer-associated genes (〉99% sensitivity), which was also negative. Clinical work-up of the patient failed to reveal abnormal masses in the breast or elsewhere. The clinical history, histological appearance, immunohistochemical profile (including negative CK7 and positive NSE, c-kit and CD10) as well as a negative RT-PCR renders almost null the possibility of a breast carcinoma and supports a diagnostic of melanoma in this case. Cases like ours may be easily misclassified unless a concerted approach is used to reach the correct diagnosis.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...