@article{GlutschWobserSchillingetal.2022,
  author    = {Glutsch, Valerie and Wobser, Marion and Schilling, Bastian and Gesierich, Anja and Goebeler, Matthias and Kneitz, Hermann},
  title     = {PRAME expression as helpful immunohistochemical marker in rhabdoid melanoma},
  series = {Dermatopathology},
  volume    = {9},
  journal   = {Dermatopathology},
  number    = {2},
  issn      = {2296-3529},
  doi       = {10.3390/dermatopathology9020019},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-284115},
  pages     = {148 -- 157},
  year      = {2022},
  abstract  = {Background: Rhabdoid melanoma is a rare variant of malignant melanoma with characteristic cytomorphologic features. Due to the potential loss of conventional melanocytic markers, histopathologic diagnosis is often challenging. We hypothesize that immunostaining for PReferentially expressed Antigen in MElanoma (PRAME) might have the potential to uncover the melanocytic origin of these dedifferentiated tumors. Methods: Four cases of rhabdoid primary melanomas were assessed by immunohistochemistry for expression of PRAME and conventional melanocytic markers. Immunohistochemical expression patterns were analyzed in the rhabdoid primaries and, if available, associated metastases. Results: All four cases of rhabdoid primary melanomas showed a strong nuclear positivity for PRAME, while the expression of conventional melanocytic markers S100, MART-1, SOX-10 and HMB-45 was variable between the analyzed cases. Conclusions: In summary, we report four cases of rhabdoid primary melanoma with high to intermediate expression of PRAME despite the partial and variable loss of other melanocytic markers. Hence, PRAME might facilitate the recognition of this highly aggressive entity to avoid misdiagnosis due to histopathologic pitfalls.},
  language  = {en}
}
@article{KneitzRoseGlutschetal.2022,
  author    = {Kneitz, Hermann and Rose, Christian and Glutsch, Valerie and Goebeler, Matthias},
  title     = {Recurrence of a cellular blue nevus with satellitosis — a diagnostic pitfall with clinical consequences},
  series = {Dermatopathology},
  volume    = {9},
  journal   = {Dermatopathology},
  number    = {4},
  issn      = {2296-3529},
  doi       = {10.3390/dermatopathology9040042},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-297436},
  pages     = {361 -- 367},
  year      = {2022},
  abstract  = {Blue nevus is a benign melanocytic lesion, typically asymptomatic and of unknown etiology. Several histologic and clinical variants have been distinguished, the most frequent being common blue nevus, cellular blue nevus, and combined blue nevus. Although melanocytic nevi with a satellite lesion are usually suggestive of locally advanced malignant melanoma, very few cases of blue nevi with satellite lesions have been reported. The diagnosis of common or cellular blue nevi is generally straightforward; however, the presence of structures such as irregular edges or satellitosis are highly suggestive for malignancy, and differential diagnoses such as locally advanced malignant melanoma and malignant blue nevus should be considered. Recurrent blue nevi can display atypical features not seen in the primary lesion, such as pleomorphism and mitotic activity. They usually tend to follow a benign course; however, in some cases, recurrence may indicate malignant transformation. We here report the unique case of a 64-year-old woman with a recurrent cellular blue nevus accompanied by satellite lesions. Such a biological behavior resulting in a clinical presentation as a melanoma-like lesion is a rarity in blue nevus and has not been described before.},
  language  = {en}
}