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The synchronous occurrence of melanomas of varying histological types is an uncommon event, with reported incidences ranging from 0.2% to 8.6%. We present the case of a patient diagnosed with Stage IIB nodular melanoma and Stage IIIC epithelioid cell melanoma within a 3-month period. After surgical excision of both lesions, lymph node enlargement was observed in the obturator region, indicating metastatic spread. As a result, combined immunotherapy with nivolumab and ipilimumab was initiated. Nivolumab and ipilimumab were administered at doses of 1 and 3 mg/kg, respectively, every 3 weeks for a total of four doses. Thereafter, treatment was continued with nivolumab alone at a dose of 3 mg/kg every 2 weeks. The patient underwent three cycles of immunotherapy, initially combined with intravenous methylprednisolone, later transitioned to an oral regimen with dexamethasone. The patient initially demonstrated a favorable clinical response without adverse effects. However, after the third infusion, severe diarrhea developed, leading to daily fluid losses exceeding 8 L and associated hypokalemia. Therefore, methylprednisolone was administered intravenously (2 mg/kg/day). Additionally, the patient experienced a splenic infarction that resolved spontaneously without resulting in asplenia. At the most recent follow-up evaluation, no lymph node enlargement was detected, and surveillance continues at 3-month intervals. Although rare, the simultaneous emergence of melanomas at distinct anatomical sites underscores the necessity for increased patient vigilance and comprehensive clinical monitoring to facilitate early detection and timely intervention. Prompt initiation of targeted immunotherapy may improve patient prognosis and outcomes.
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http://dx.doi.org/10.1155/crom/6396505 | DOI Listing |
Oncol Ther
September 2025
Department of Infectious Diseases, Nord Franche-Comté Hospital, Belfort, France.
This is the first documented case of recurrent, severe, and highly inflammatory panmyelitis induced by pembrolizumab. A 41-year-old woman with nodular melanoma developed tetraparesis after three cycles of pembrolizumab treatment. Spinal magnetic resonance imaging (MRI) revealed extensive longitudinal panmyelitis, and cerebrospinal fluid analysis showed markedly elevated cell counts (3900/mm).
View Article and Find Full Text PDFGeorgian Med News
June 2025
1Onkoderma - Clinic for Dermatology, Venereology and Dermatologic Surgery, Sofia, Bulgaria.
Acral lentiginous melanoma (ALM) is a rare type of cutaneous malignant melanoma, predominantly affecting the acral sites and subungual regions of the upper and lower extremities. Unlike other melanoma types, UV exposure is not considered as significant etiological factor. Instead, mechanical stress, particularly traumatic injury, is recognized as a potential contributor to ALM development, especially in weight-bearing areas such as the sole.
View Article and Find Full Text PDFCancers (Basel)
August 2025
Unit of Cancer Genetics, Istituto di Ricerca Genetica e Biomedica-Consiglio Nazionale delle Ricerche (IRGB-CNR), Traversa La Crucca 3, 07100 Sassari, Italy.
: The clinical, histopathological, and dermoscopic features may be associated with melanoma mutational status. The aims of the study were to assess the clinical, histopathological, and dermoscopic features of melanoma to identify their correlation with , , and cell cycle genes' mutational status in melanoma. : The clinical, histopathological information, dermoscopic images, and genomic DNA of 55 histopathologically diagnosed primary cutaneous melanomas were retrospectively analyzed.
View Article and Find Full Text PDFCureus
July 2025
Dermatology, Hospital General "Dr. Manuel Gea González", Mexico City, MEX.
Acral amelanotic melanoma (AM) is a rare and aggressive melanoma subtype that frequently presents with a diagnostic delay due to its atypical characteristics. Sporotrichoid spread, suggesting lymphatic dissemination, is rarely seen. Vitiligo, although usually benign, may signal underlying malignancy when appearing de novo in older adults.
View Article and Find Full Text PDFReports (MDPI)
August 2025
Department of Plastic Surgery and Burns Treatment, Copenhagen University Hospital, 2100 Copenhagen, Denmark.
: Osteonevus of Nanta is a rare histological phenomenon characterized by bone formation within a benign melanocytic nevus, most commonly in intradermal nevi of the head and neck. Although osteonevus of Nanta is rare, ossification in a cellular blue nevus is even more uncommon. To date, only one case of a cellular blue nevus with ossification has been documented.
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