Acta Dermato-Venereologica 97-10CompleteContent | Seite 30

1252 SHORT COMMUNICATION Coincident Metastatic Melanoma and Merkel Cell Carcinoma with Complete Remission on Treatment with Pembrolizumab Alexander THIEM 1,2 , Hermann KNEITZ 1 , Patrick SCHUMMER 1 , Stefan HERZ 3 , David SCHRAMA 1 , Roland HOUBEN 1 , Matthias GOEBELER 1 , Bastian SCHILLING 1 and Anja GESIERICH 1 Department of Dermatology, Venereology and Allergology, University Hospital Würzburg, Josef-Schneider-Straße 2, DE-97080 Würzburg, Comprehensive Cancer Center Mainfranken, and 3 Department of Diagnostic and Interventional Radiology, University Hospital Würzburg, Würzburg, Germany. E-mail: thiem_a@ukw.de 1 2 Accepted Jul 31, 2017; Epub ahead of print Aug 1, 2017 Patients with metastatic melanoma or Merkel cell carci- noma (MCC) share a poor prognosis (1, 2). In recent years, immune checkpoint inhibitors have significantly advanced the treatment of immunogenic tumours (3). The anti-programmed cell death protein 1 (PD-1) antibodies pembrolizumab and nivo- lumab have been approved for the treatment of advanced melanoma. Clinical trials have provided evidence that pembrolizumab (4) as well as the anti-programmed death-ligand 1 (PD-L1) antibody avelumab (5) are ef- fective in the treatment of advanced MCC, with avelumab approved by the US Food and Drug Administration. We report here on a patient presenting with both metasta- tic melanoma and MCC who experienced complete remission of both on treatment with pembrolizumab. endocrine primary. However, a suspicious pancreatic lesion (Fig. 1J) was biopsied and a melanoma metastasis diagnosed based on morphology and IHC (MART-1- and HMB45-positive; nuclear CASE REPORT In July 2012, a 70-year-old man was diagnosed with a metastatic melanoma. A swelling of the right axilla was removed by surgery. Based on morphology and immunohistochemistry (IHC), an amelanotic lymph node metastasis, 5 cm in diameter, with occult primary was diagnosed (Fig. 1 A–C). Level I/II lymph node dissection (0/23 nodes positive) was conducted, and he received adjuvant radiotherapy of 50 Gy. Computed tomo- graphy (CT) scans performed initially showed no additional metastases. Follow-up was carried out in accordance with national guidelines. In April 2016 CT revealed newly enlarged right inguinal and iliac lymph nodes. A systematic lymphadenectomy was conducted. To our surprise, initial pathological review of the dissected tissue detected infiltrates of neuroen- docrine carcinoma in 7 of 20 inguinal and 8 of 20 iliac lymph nodes (Fig. 1D). IHC revealed “dot-like” positivity for pan-cytokeratin (AE1/3) and CK20, while TTF1, MITF, MART1 and HMB45 were negative (Fig. 1E). Finally, diag- nosis of MCC was made and further sustained by strong positive immunolabelling for Merkel cell polyomavirus (MCPyV) Large T antigen (clone CM2B4; Fig. 1F). No primary MCC was recor- ded in the patient’s medical history or found on clinical examination. Endoscopy of the upper and lower intestine did not reveal an internal neuro- doi: 10.2340/00015555-2757 Acta Derm Venereol 2017; 97: 1252–1254 Fig. 1. (Immuno-)histological and radiological findings. (A–C) Amelanotic lymph node melanoma metastasis from the right axilla. (A) Haematoxylin and eosin (H&E) staining with atypical melanocytes positive for (B) MART-1 and (C) S100. (D–F) Iliac MCC lymph node metastasis with round oval tumor cells containing (D) sparse cytoplasm and granular chromatin on H&E staining with (E) „dot-like“-positivity for CK20 and (F) expression of Merkel cell polyomavirus Large T antigen (MCPyV LT, stained with antibody clone CM2B4). (G-I) Both the axillary lymph node metastasis (G) as well as the iliac MCC metastasis (H) are negative for PD-L1 (immunolabelled with antibody clone E1L3N, tonsillar tissue served as positive control for PD-L1 (I)). Magnification H&E 200x (A, D), all others 400x). (J–L) CT scans demonstrating pancreatic melanoma metastasis (J) as well as an parailiac MCC metastasis before (K) and after 7 applications of pembrolizumab (L). Arrow heads indicate metastases. This is an open access article under the CC BY-NC license. www.medicaljournals.se/acta Journal Compilation © 2017 Acta Dermato-Venereologica.