Publications by authors named "Alexandra Matter"

Article Synopsis
  • The study presents the largest series of granulomatous pigmented purpuric dermatosis (GPPD), a rare skin condition that can mimic other serious diseases like cutaneous T-cell lymphoma.
  • It involves analyzing the histopathological features of nine GPPD cases compared to ten other types of pigmented purpuric dermatoses.
  • The findings indicate GPPD primarily affects adult males' lower extremities and shows distinct histological traits, including a specific immune cell profile.
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Melanoma can be classified based on the detection of relevant oncogenic driver mutations. These mutations partially determine a patient's treatment options. MEK inhibitors have demonstrated little efficacy in patients with NRAS-mutated melanoma owing to primary and secondary resistance.

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Switching from immunotherapy to targeted therapy in metastasized melanoma can be complicated by a cytokine release syndrome (CRS). CRS is a serious complication, which is induced by high levels of circulating cytokines, associated with T-cell engagement and proliferation, and results in a constellation of symptoms with variable organ involvement. We report 2 patients with BRAF V600 mutant melanoma who were previously treated with anti-PD-1±anti-LAG-3 antibodies and were switched to BRAF/MEK-inhibitors because of progressive disease.

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The descriptive term hybrid peripheral nerve sheath tumor refers to any neoplasm of the neurilemmal apparatus composed of more than one pathologically defined tumoral equivalent derived from its constituent cells. Within this uncommon nosological category, participation of granular cell tumor - a neoplasm of modified Schwann cells - has been reported only exceptionally. We describe a hitherto not documented variant composed of an organoid mixture of granular cell tumor and perineurioma with plexiform growth.

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