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2. Indeterminate DC histiocytosis is distinct from LCH and often associated with other hematopoietic neoplasms

Author

Ozkaya, Neval, Melloul Benizri, Sarah, Venkataraman, Girish, Karai, Laszlo J., Fraitag, Sylvie, Razanamahery, Jérôme, Pittaluga, Stefania, Battistella, Maxime, Pack, Svetlana, Le Pelletier, François, Xi, Liqiang, Moreau, Anne, Lee, Ina, Hélias-Rodzewicz, Zofia, Donadieu, Jean, Haroche, Julien, Raffeld, Mark, Jaffe, Elaine S., and Emile, Jean-François

Published
2024
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3. Radiotherapy in cutaneous lymphomas: Recommendations from the EORTC cutaneous lymphoma tumour group

Author

Elsayad, Khaled, Guenova, Emmanuella, Assaf, Chalid, Nicolay, Jan P., Trautinger, Franz, Stadler, Rudolf, Waldstein, Cora, Boterberg, Tom, Meijnders, Paul, Kirova, Youlia, Dobos, Gabor, Duque-Santana, Victor, Riggenbach, Elena, Elsheshtawy, Wael, Niezink, Anne, Papadavid, Evangelia, Scarisbrick, Julia, Vermeer, Maarten, Neelis, Karen J., Bagot, Martine, Battistella, Maxime, Quaglino, Pietro, Knobler, Robert, Kempf, Werner, Maklad, Ahmed, Adeberg, Sebastian, Kouloulias, Vassilis, Simontacchi, Gabriele, Corradini, Stefanie, König, Laila, Eich, Hans Theodor, Cowan, Richard, and Correia, Dora

Published
2024
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4. Wnt/β-Catenin–Activated Nonpilomatrical Carcinoma of the Skin: A Case Series

Author

Kervarrec, Thibault, Cheok Lei, Kuan, Sohier, Pierre, Macagno, Nicolas, Jullie, Marie-Laure, Frouin, Eric, Goto, Keisuke, Taniguchi, Kohei, Hamard, Aymeric, Taillandier, Antoine, Tallet, Anne, Bonenfant, Christine, Sahin, Yusuf, Barry, Fatoumata, Taibjee, Saleem, Cokelaere, Kristof, Houben, Roland, Schrama, David, Nardin, Charlee, Aubin, Francois, Doucet, Laurent, Pissaloux, Daniel, Tirode, Franck, Fouchardière, Arnaud de la, Balme, Brigitte, Laurent-Roussel, Sara, Becker, Jürgen C., von Deimling, Andreas, Samimi, Mahtab, Cribier, Bernard, Battistella, Maxime, Calonje, Eduardo, and Guyétan, Serge

Published
2024
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7. Real-life efficacy of immunotherapy for Sézary syndrome: a multicenter observational cohort study

Author

Bozonnat, Alizée, Beylot-Barry, Marie, Dereure, Olivier, D’Incan, Michel, Quereux, Gaëlle, Guenova, Emmanuella, Perier-Muzet, Marie, Dalle, Stephane, Grange, Florent, Viguier, Manuelle-Anne, Ram-Wolff, Caroline, Feldmeyer, Laurence, Beltraminelli, Helmut, Bonnet, Nathalie, Amatore, Florent, Maubec, Eve, Franck, Nathalie, Machet, Laurent, Chasset, François, Brunet-Possenti, Florence, Bouaziz, Jean-David, Battistella, Maxime, Donzel, Marie, Pham-Ledard, Anne, Bejar, Claudia, Moins-Teisserenc, Hélène, Mourah, Samia, Saiag, Philippe, Hainaut, Ewa, Michel, Catherine, Bens, Guido, Adamski, Henri, Aubin, François, Boulinguez, Serge, Joly, Pascal, Tedbirt, Billal, Templier, Isabelle, Troin, Laura, Montaudié, Henri, Ingen-Housz-Oro, Saskia, Faiz, Sarah, Mortier, Laurent, Dobos, Gabor, Bagot, Martine, Resche-Rigon, Matthieu, Montlahuc, Claire, Serret-Larmande, Arnaud, and de Masson, Adèle

Published
2024
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9. SOX10-Internal Tandem Duplications and PLAG1 or HMGA2 Fusions Segregate Eccrine-Type and Apocrine-Type Cutaneous Mixed Tumors

Author

Macagno, Nicolas, Kervarrec, Thibault, Thanguturi, Soumanth, Sohier, Pierre, Pissaloux, Daniel, Mescam, Lenaïg, Jullie, Marie-Laure, Frouin, Eric, Osio, Amelie, Faisant, Monique, Le Loarer, François, Cribier, Bernard, Calonje, Eduardo, Luna, Evelyn Vanesa Erazo, Massi, Daniela, Goto, Keisuke, Nishida, Haruto, Paindavoine, Sandrine, Houlier, Aurelie, Tantot, Juliet, Benzerdjeb, Nazim, Tirode, Franck, De la Fouchardière, Arnaud, and Battistella, Maxime

Published
2024
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10. Re-evaluation of the concept of basaloid follicular hamartoma associated with naevoid basal cell carcinoma syndrome: a morphological, immunohistochemical and molecular study

Author

Barbieux, Simon, Jouenne, Fanélie, Machet, Marie-Christine, Fraitag, Sylvie, Macagno, Nicolas, Battistella, Maxime, Cribier, Bernard, Sohier, Pierre, Laurent-Roussel, Sara, Carlotti, Agnès, Beltzung, Fanny, Jullié, Marie-Laure, Moulonguet, Isabelle, Basset-Seguin, Nicole, Deschamps, Lydia, Mourah, Samia, Samimi, Mahtab, Guyétant, Serge, and Kervarrec, Thibault

Published
2024
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11. Allogeneic transplantation in advanced cutaneous T-cell lymphomas (CUTALLO): a propensity score matched controlled prospective study

Author

de Masson, Adèle, Beylot-Barry, Marie, Ram-Wolff, Caroline, Mear, Jean-Baptiste, Dalle, Stéphane, d'Incan, Michel, Ingen-Housz-Oro, Saskia, Orvain, Corentin, Abraham, Julie, Dereure, Olivier, Charbonnier, Amandine, Cornillon, Jérôme, Longvert, Christine, Barete, Stéphane, Boulinguez, Serge, Wierzbicka-Hainaut, Ewa, Aubin, François, Rubio, Marie-Thérèse, Bernard, Marc, Schmidt-Tanguy, Aline, Houot, Roch, Pham-Ledard, Anne, Michonneau, David, Brice, Pauline, Labussière-Wallet, Hélène, Bouaziz, Jean-David, Grange, Florent, Moins-Teisserenc, Hélène, Jondeau, Katayoun, Michel, Laurence, Mourah, Samia, Battistella, Maxime, Daguindau, Etienne, Loschi, Michael, Picard, Alexandra, Franck, Nathalie, Maillard, Natacha, Huynh, Anne, Nguyen, Stéphanie, Marçais, Ambroise, Chaby, Guillaume, Ceballos, Patrice, Le Corre, Yannick, Maury, Sébastien, Bay, Jacques-Olivier, Adamski, Henri, Bachy, Emmanuel, Forcade, Edouard, Socié, Gérard, Bagot, Martine, Chevret, Sylvie, Peffault de Latour, Régis, and de Latour, Régis Peffault

Published
2023
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12. IgA vasculitis with underlying monoclonal IgA gammopathy: innovative therapeutic approach targeting plasma cells. A case series

Author

Hankard, Antoine, Ingen-Housz-Oro, Saskia, El Karoui, Khalil, Paule, Romain, Lioger, Bertrand, Brihaye, Benoit, Battistella, Maxime, Jobard, Stéphanie, Magnant, Julie, Diot, Elisabeth, Bigot, Adrien, Ferreira-Maldent, Nicole, Deriaz, Sophie, Cook, Ann-Rose, Henique, Hélène, Maillot, Francois, Aouba, Achille, and Audemard-Verger, Alexandra

Published
2022
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13. Sweat Gland Tumors Arising on Acral Sites: A Molecular Survey

Author

Kervarrec, Thibault, Tallet, Anne, Macagno, Nicolas, de la Fouchardière, Arnaud, Pissaloux, Daniel, Tirode, Franck, Bravo, Ignacio G., Nicolas, Alain, Baulande, Sylvain, Sohier, Pierre, Balme, Brigitte, Osio, Amélie, Jullie, Marie-Laure, Moulonguet, Isabelle, Bonsang, Benjamin, Tournier, Emilie, Herfs, Michael, Frouin, Eric, Zidan, Anoud, Calonje, Eduardo, Berthon, Patricia, Touzé, Antoine, Seris, Alice, Mortier, Laurent, Jouary, Thomas, Cribier, Bernard, and Battistella, Maxime

Published
2023
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14. Digital Papillary Adenocarcinoma in Nonacral Skin: Clinicopathologic and Genetic Characterization of 5 Cases

Author

Kervarrec, Thibault, Imbeaud, Sandrine, Veyer, David, Pere, Helene, Puech, Julien, Pekár-Lukacs, Agnes, Markiewicz, Dorota, Coutts, Michael, Tallet, Anne, Collin, Christine, Berthon, Patricia, Bravo, Ignacio G., Seris, Alice, Jouary, Thomas, Macagno, Nicolas, Touzé, Antoine, Cribier, Bernard, Battistella, Maxime, and Calonje, Eduardo

Published
2023
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15. Genomic profiling of a skin adnexal carcinomas cohort using a comprehensive high throughput sequencing approach

Author

Louveau, Baptiste, primary, Nakouri, Ines, additional, Jouenne, Fanélie, additional, Baroudjian, Barouyr, additional, Sadoux, Aurélie, additional, Da Meda, Laetitia, additional, Osio, Amélie, additional, Reinhart, Fanny, additional, Robert, Julien, additional, Herms, Florian, additional, Cribier, Bernard, additional, Mortier, Laurent, additional, Jouary, Thomas, additional, Basset Seguin, Nicole, additional, Lebbé, Céleste, additional, Mourah, Samia, additional, and Battistella, Maxime, additional

Published
2024
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21. Macrophage-derived CXCL9 and CXCL11, T-cell skin homing, and disease control in mogamulizumab-treated CTCL patients

Author

de Masson, Adèle, Darbord, Delphine, Dobos, Gabor, Boisson, Marie, Roelens, Marie, Ram-Wolff, Caroline, Cassius, Charles, Le Buanec, Hélène, de la Grange, Pierre, Jouenne, Fanélie, Louveau, Baptiste, Sadoux, Aurélie, Bouaziz, Jean-David, Marie-Cardine, Anne, Bagot, Martine, Moins-Teisserenc, Hélène, Mourah, Samia, and Battistella, Maxime

Published
2022
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22. Metastatic perirectal PEComa treated by checkpoint inhibitor immunotherapy and multimodal treatment: case report and review of the literature.

Author

Rémond, Maxime, Pachev, Atanas, Battistella, Maxime, Gandon, Camille, Mourah, Samia, Madelaine, Isabelle, Maggiori, Léon, Benadon, Bethsabée, Hammoudi, Nassim, Lourenço, Nelson, and Aparicio, Thomas

Abstract

Malignant PEComas are an extremely rare subtype of soft tissue sarcomas. Here, we report the case of a man presenting with a perirectal PEComa and liver metastasis. Since the tumor harbored a tumor mutational burden of 23/Mb and a programmed death-ligand 1 tumor positivity score of 50%, the patient was treated with pembrolizumab as a second line of systemic therapy, in combination with everolimus. This combined therapy led to a near-complete response of the primary tumor and a partial response of the metastasis. Radioembolization of the liver metastasis was performed due to isolated liver progression, and the pelvic tumor was treated by radiotherapy because of pelvic symptoms. The disease is still stable after 13 months of pembrolizumab plus everolimus and multimodal treatment. This case shows that malignant PEComas can display molecular features associated with sensitivity to checkpoint inhibitors. The use of checkpoint inhibitors may be a relevant therapeutic strategy in these patients. It is also the first report on selective internal radiation therapy in PEComas. Plain language summary: A case of a patient with metastatic PEComa of the rectum, a very rare tumor type, treated by immunotherapy in combination with local treatments This article reports the case of a patient presenting with a very rare tumor type called "PEComa". The tumor originated from the rectum and had disseminated to the liver. Since this tumor is very rare, there is a lack of knowledge on which treatments to use, and every case reporting the use of new treatments in PEComas is helpful. Here, the tumor displayed molecular alterations that suggested that it would respond to immunotherapy, such as a high number of mutations. Therefore, the patient was treated with an immunotherapy called pembrolizumab, in combination with another medication (everolimus). The rectal tumor nearly disappeared under treatment, and the liver metastasis decreased in size. The patient had radiotherapy of the rectum because of rectal bleeding. For the liver metastasis we used another technique called radioembolization, that consists in delivering radioactive compounds directly in the metastasis through the bloodstream. Now, he has received immunotherapy for 13 months and the disease is still under control. This case shows that immunotherapy can be a good treatment option in PEComas. It is also the first time that a medical team reports the using radioembolization to treat a PEComa. [ABSTRACT FROM AUTHOR]

Published
2024
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25. Porocarcinomas with PAK1/2/3 fusions: a series of 12 cases

Author

Kervarrec, Thibault, primary, Westphal, Danna, additional, Pissaloux, Daniel, additional, Legrand, Mélanie, additional, Tirode, Franck, additional, Neuhart, Anne, additional, Drouot, Francoise, additional, Becker, Jürgen C, additional, Macagno, Nicolas, additional, Seris, Alice, additional, Jouary, Thomas, additional, Beltzung, Fanny, additional, Jullie, Marie‐Laure, additional, Harms, Paul W, additional, Cribier, Bernard, additional, Mourah, Samia, additional, Jouenne, Fanélie, additional, Fromont, Gaelle, additional, Louveau, Baptiste, additional, Mancini, Maxence, additional, Kazakov, Dmitry V, additional, de la Fouchardière, Arnaud, additional, and Battistella, Maxime, additional

Published
2024
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27. Cutaneous clonal mature plasmacytoid dendritic cell dermatosis in patients with myeloid neoplasms

Author

Mahévas, Thibault, primary, Osio, Amélie, additional, Larcher, Lise, additional, Clappier, Emmanuelle, additional, Kempf, Werner, additional, Adès, Lionel, additional, Fenaux, Pierre, additional, Sébert, Marie, additional, Delaleu, Jérémie, additional, Jachiet, Marie, additional, Cordoliani, Florence, additional, Charvet, Estelle, additional, Carpentier, Olivier, additional, Itzykson, Raphaël A., additional, Weinborn, Marie, additional, Mardare, Nicoleta, additional, Marco-Bonnet, Joséfina, additional, de Masson, Adèle, additional, Duployez, Nicolas, additional, Huynh, Tony, additional, Bouaziz, Jean-David, additional, Vignon-Pennamen, Marie-Dominique, additional, and Battistella, Maxime, additional

Published
2024
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30. Impact of blood tumour clone frequency on time to next treatment in mycosis fungoides

Author

Lazaridou, Ingrid, primary, Alqahtani, Mohammed, additional, Louveau, Baptiste, additional, Ram‐Wolff, Caroline, additional, Alharbi, Bader, additional, Al Hage, Jana, additional, Dumont, Maëlle, additional, Bouaziz, Jean‐David, additional, Bagot, Martine, additional, Moins‐Teisserenc, Hélène, additional, Rivet, Jacqueline, additional, Battistella, Maxime, additional, Mourah, Samia, additional, and de Masson, Adèle, additional

Published
2024
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31. Targeting TGF-beta activation in cutaneous T-cell lymphomas

Author

GIUSTINIANI, Jérôme, primary, Anh TA, Van, additional, Belkhelouat, Sadjia, additional, BATTISTELLA, Maxime, additional, OUAHBI, Dina, additional, RAM-WOLFF, Caroline, additional, LOUVEAU, Baptiste, additional, MOURAH, Samia, additional, BAGOT, Martine, additional, MOINS-TEISSERENC, Hélène, additional, Ortonne, Nicolas, additional, BENSUSSAN, Armand, additional, and MASSON, Adèle DE., additional

Published
2024
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35. Hidrocystoma-like tumours with RETor ALKfusion: a study of four cases

Author

Goto, Keisuke, Kervarrec, Thibault, Tallet, Anne, Macagno, Nicolas, Pissaloux, Daniel, Fouchardière, Arnaud de la, Battistella, Maxime, Kajiwara, Manami, Nagao, Toshitaka, Fujita, Ikuo, Kajimoto, Kazuyoshi, Goto, Hiroshi, Matsumura, Hajime, and Takai, Toshihiro

Abstract

Hidrocystoma is thought to be a benign retention cyst of sweat ductal units. The lesion is usually located in the periorbital skin; however, lesions with similar histopathological features are rarely observed in extra-facial sites. Herein, we present four cases of hidrocystoma-like tumours in extra-facial skin sites that harboured a RETor ALKrearrangement. This study features a 67-year-old female with a 10 mm-sized digital tumour (Case 1), a 62-year-old male with an 8 mm-sized clavicular tumour (Case 2), a 61-year-old male with a 19 mm-sized digital tumour (Case 3), and an 11-year-old female with a 10 mm-size lower leg tumour (Case 4) as well as five control cases (Cases 5–9) of classical periorbital hidrocystoma. In Cases 1–4, multicystic tumours comprising a two-cell layer of inner cuboidal ductoglandular (p63− and SOX10+/−) and outer flat myoepithelial (p63+ and SOX10+) cells were observed. The inner ductoglandular tumour cells exhibited micropapillary projections and Roman bridging structures. No apparent atypical cells were observed. NCOA4::RETin Cases 1 and 3, CCDC6::RETin Case 2, and SLC12A2::ALKin Case 4 were revealed by next-generation sequencing or Sanger sequencing. In contrast, control cases of classical hidrocystoma (Cases 5–9) did not show intracystic proliferation, abundant cytoplasm, ALK immunoreactivity, or NCOA4::RETdetection in the tumour cells. RET/ALK-rearranged hidrocystoma-like tumours are tumour entities that can be distinguished from classical hidrocystoma. This RET/ALK-rearranged neoplasm is benign and is frequently observed in the digits. Future studies will establish the concept, detailed clinicopathological characteristics, and genetic variations of hidrocystoma-like tumours.

Published
2024
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36. Exploring the molecular landscape of cutaneous mixed tumors characterized by TRPS1::PLAG1 gene fusion.

Author

Alsugair, Ziyad, Donzel, Marie, Macagno, Nicolas, Tantot, Juliet, Harou, Olivier, Battistella, Maxime, Sohier, Pierre, Kervarrec, Thibault, de la Fouchardière, Arnaud, Balme, Brigitte, Champagnac, Anne, Lanic, Marie‐Delphine, Lopez, Jonathan, Laé, Marick, Descotes, Françoise, Tirode, Franck, Pissaloux, Daniel, Thamphya, Brice, Costes‐Martineau, Valérie, and Benzerdjeb, Nazim

Abstract

The histological similarities between pleomorphic adenomas (PAs) and cutaneous mixed tumors (CMTs) found in certain facial regions can create a diagnostic challenge. Molecular findings reveal common genetic profiles, particularly PLAG1 rearrangements in both PA and CMT. Although molecular distinctions have received limited attention, our observations indicate multiple cases of CMTs carrying the TRPS1::PLAG1 fusion. This clinical experience has driven our investigation into the potential diagnostic utility of TRPS1::PLAG1 fusions for determining tumor origin. Two cohorts consisting of 46 cases of CMT and 45 cases of PA of the salivary glands were obtained from French institutions and reviewed by specialists in each subspecialty. RNA sequencing analysis was conducted to identify the molecular features of cases harboring PLAG1. Clinical, pathological, and molecular data were collected. In this study, cases of CMT exhibited recurrent gene fusions, primarily TRPS1::PLAG1 (74%). These tumors shared characteristic histological features, including tubuloductal differentiation in 55% of cases and squamous metaplasia in varying proportions. In contrast, cases of PA had gene fusions involving PLAG1 with various gene partners, with only one case in which TRPS1::PLAG1 was identified. This disparity was also observed at the transcriptomic level between TRPS1::PLAG1 CMTs and other tumors. However, TRPS1 immunostaining did not correlate with TRPS1::PLAG1 fusion. In conclusion, we report that recurrent TRPS1::PLAG1 fusion CMTs exhibit similar characteristic histological features, including tubuloductal differentiation that is associated with squamous metaplasia in around half of cases. Detection of this fusion could be valuable in correctly identifying the origin of these tumors. © 2024 The Pathological Society of Great Britain and Ireland. [ABSTRACT FROM AUTHOR]

Published
2024
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37. Citrullinated Histone H3, a Marker for Neutrophil Extracellular Traps, Is Associated with Poor Prognosis in Cutaneous Squamous Cell Carcinoma Developing in Patients with Recessive Dystrophic Epidermolysis Bullosa.

Author

Ragot, Hélène, Gaucher, Sonia, Bonnet des Claustres, Mathilde, Basset, Justine, Boudan, Rose, Battistella, Maxime, Bourrat, Emmanuelle, Hovnanian, Alain, and Titeux, Matthias

Subjects
SQUAMOUS cell carcinoma, RISK assessment, SKIN diseases, RESEARCH funding, EPIDERMOLYSIS bullosa, NEUTROPHILS, CELL physiology, TUMOR markers, RETROSPECTIVE studies, LYMPHOCYTES, DESCRIPTIVE statistics, HISTONES, LONGITUDINAL method, EXTRACELLULAR space, CANCER patient psychology, COMPARATIVE studies, INTERLEUKINS, BLOOD, DISEASE risk factors
Abstract

Simple Summary: Recessive dystrophic epidermolysis bullosa (RDEB) is a rare and severe hereditary skin disease characterized by skin and mucosa fragility. RDEB patients are predisposed to the development of life-threatening cutaneous squamous cell carcinoma (SCC). In this study, we investigated the immune profiles of SCCs occurring in a cohort of RDEB patients and compared them with clinical, histopathological and prognostic features. We describe two distinct clinical outcomes in RDEB patients with cutaneous SCCs. A majority of RDEB patients had local and not rapidly life-threatening SCC, while others developed early aggressive and metastatic SCCs. The high-risk primary RDEB-SCC was associated with a tumor microenvironment displaying a higher neutrophil-to-lymphocyte infiltration ratio. Increased levels of citrullinated histone H3, a marker of neutrophil extracellular traps (NET), were detected in tumoral skin and in the serum of RDEB patients with high-risk primary SCC. Recessive dystrophic epidermolysis bullosa (RDEB) is a rare severe hereditary skin disease characterized by skin and mucosa fragility, resulting in blister formation. The most severe complication in RDEB patients is the development of cutaneous squamous cell carcinoma (SCC), leading to premature death. There is a great deal of evidence suggesting a permissive tumor microenvironment (TME) as a driver of SCC development in RDEB patients. In a cohort of RDEB patients, we characterized the immune profiles of RDEB-SCCs and compared them with clinical, histopathological, and prognostic features. RDEB-SCCs were subdivided into four groups based on their occurrence (first onset or recurrences) and grading according to clinical, histopathological parameters of aggressiveness. Thirty-eight SCCs from 20 RDEB patients were analyzed. Five RDEB patients experienced an unfavorable course after the diagnosis of the first SCC, with early recurrence or metastasis, whereas 15 patients developed multiple SCCs without metastasis. High-risk primary RDEB-SCCs showed a higher neutrophil-to-lymphocyte ratio in the tumor microenvironment and an increased proportion of neutrophil extracellular traps (NETs). Additionally, citrullinated histone H3, a marker of NETs, was increased in the serum of RDEB patients with high-risk primary SCC, suggesting that this modified form of histone H3 may serve as a potential blood marker of unfavorable prognosis in RDEB-SCCs. [ABSTRACT FROM AUTHOR]

Published
2024
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39. A Sub-Group of Kidney-Transplant Recipients with Highly Aggressive Squamous Cell Carcinoma Expressing Phosphorylated Serine392p53

Author

Hamdan, Diaddin, primary, Gardair, Charlotte, additional, Pamoukdjian, Frédéric, additional, Peraldi Gardin, Marie-Noëlle, additional, Nakouri, Inès, additional, Leboeuf, Christophe, additional, Janin, Anne, additional, Lebbé, Céleste, additional, Battistella, Maxime, additional, and Bousquet, Guilhem, additional

Published
2024
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41. Erratum to ‘Molecular profiling of anal Paget’s disease and underlying anal adenocarcinoma highlights their common origin’ [EJC Skin Cancer 1 (2023) 100002]

Author

Bellahsen-Harrar, Yaëlle, primary, Boisson, Marie, additional, Louveau, Baptiste, additional, Baroudjian, Barouyr, additional, Aparicio, Thomas, additional, Ferré, Valentine, additional, Parc, Yann, additional, Sadoux, Aurélie, additional, Jouenne, Fanélie, additional, Battistella, Maxime, additional, Lebbé, Céleste, additional, and Mourah, Samia, additional

Published
2024
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42. Two cases of Dupilumab responsive Kimura disease

Author

Battesti, Gilles, primary, Jachiet, Marie, additional, Lepelletier, Clémence, additional, Petit, Antoine, additional, Vignon-Pennamen, Marie-Dominique, additional, Cassius, Charles, additional, de Masson, Adèle, additional, Battistella, Maxime, additional, Bagot, Martine, additional, Bouaziz, Jean David, additional, and Mahévas, Thibault, additional

Published
2023
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44. Transcriptomic Landscape of Prurigo Nodularis Lesional Skin CD3+ T Cells Using Single-Cell RNA Sequencing

Author

Calugareanu, Andreea, primary, Specque, Florian, additional, Demouche, Sarah, additional, Grolleau, Chloe, additional, Dobos, Gabor, additional, Merandet, Marine, additional, Bergerat, David, additional, Peltier, Sandy, additional, Jachiet, Marie, additional, Cassius, Charles, additional, Mahevas, Thibault, additional, Saussine, Anne, additional, How-Kit, Alexandre, additional, Onifarasoaniaina, Rachel, additional, Serror, Kevin, additional, Bohec, Mylène, additional, Baulande, Sylvain, additional, Lepelletier, Clemence, additional, Mrad, Marc, additional, Charvet, Estelle, additional, Masson, Adèle de, additional, Boccara, David, additional, Battistella, Maxime, additional, Buanec, Hélène Le, additional, and Bouaziz, Jean-David, additional

Published
2023
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49. IPH4102, a first-in-class anti-KIR3DL2 monoclonal antibody, in patients with relapsed or refractory cutaneous T-cell lymphoma: an international, first-in-human, open-label, phase 1 trial

Author

Bagot, Martine, Porcu, Pierluigi, Marie-Cardine, Anne, Battistella, Maxime, William, Basem M, Vermeer, Maarten, Whittaker, Sean, Rotolo, Federico, Ram-Wolff, Caroline, Khodadoust, Michael S, Bensussan, Armand, Paturel, Carine, Bonnafous, Cecile, Sicard, Helene, Azim, Hatem A, Jr, and Kim, Youn H

Published
2019
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50. Pédagogie à grande échelle en ACP

Author

Bertheau, Philippe, Denize, Thomas, Calvani, Julien, Gardair, Charlotte, Jacquier, Anthony, Razafimahefa, Joëlle, Eymerit-Morin, Caroline, Perron, Émilie, Tremblay-Le May, Rosemarie, Borduas, Martin, Pote, Nicolas, Battistella, Maxime, Badoual, Cécile, Fléjou, Jean-François, Leteurtre, Emmanuelle, Uro-Coste, Emmanuelle, Buob, David, and Valmary-Degano, Séverine

Published
2019
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