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DOI 10.1097/pas.0000000000001702

Медицинская библиотека · The American journal of surgical pathology · 2021

Infantile Rhabdomyosarcomas With VGLL2 Rearrangement Are Not Always an Indolent Disease: A Study of 4 Aggressive Cases With Clinical, Pathologic, Molecular, and Radiologic Findings.

Cyrta Joanna, Gauthier Arnaud, Karanian Marie, Vieira Andre F, Cardoen Liesbeth, Jehanno Nina, Bouvet Mégane, Bouvier Corinne, Komuta Mina, Le Loarer François, Orbach Daniel, Rome Angélique, Minard-Colin Véronique, Brichard Bénédicte, Pluchart Claire, Thebaud Estelle, Renard Marleen, Pannier Stéphanie, Brisse Hervé, Petit Philippe, Benoist Camille, Schleiermacher Gudrun, Geoerger Birgit, Vincent-Salomon Anne, Fréneaux Paul, Pierron Gaëlle

Клинический случайСтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

VGLL2-rearranged rhabdomyosarcomas (RMS) are rare low-grade tumors with only favorable outcomes reported to date. We describe 4 patients with VGLL2-rearranged RMS confirmed by molecular studies, who experienced local progression and distant metastases, including 2 with fatal outcomes. Tumors were diagnosed at birth (n=3) or at 12 months of age (n=1), and were all localized at initial diagnosis, but unresectable and therefore managed with chemotherapy and surveillance. Metastatic progression occurred from 1 to 8 years from diagnosis (median, 3.5 y). Three patients experienced multimetastatic spread and one showed an isolated adrenal metastasis. At initial diagnosis, 3 tumors displaying bland morphology were misdiagnosed as fibromatosis or infantile fibrosarcoma and initially managed as such, while 1 was a high-grade sarcoma. At relapse, 3 tumors showed high-grade morphology, while 1 retained a low-grade phenotype. Low-grade primary tumors showed only very focal positivity for desmin, myogenin, and/or MyoD1, while high-grade tumors were heterogenously or diffusely positive. Whole-exome sequencing, performed on primary and relapse samples for 3 patients, showed increased genomic instability and additional genomic alterations (eg, TP53, CDKN2A/B, FGFR4) at relapse, but no recurrent events. RNA sequencing confirmed that high-grade tumors retained VGLL2 fusion transcripts and transcriptomic profiles consistent with VGLL2-rearranged RMS. High-grade samples showed a high expression of genes encoding cell cycle proteins, desmin, and some developmental factors. These 4 cases with distinct medical history imply the importance of complete surgical resection, and suggest that RMS-type chemotherapy should be considered in unresectable cases, given the risk of high-grade transformation. They also emphasize the importance of correct initial diagnosis.

Для цитирования: Cyrta Joanna, Gauthier Arnaud, Karanian Marie, Vieira Andre F, Cardoen Liesbeth, Jehanno Nina, Bouvet Mégane, Bouvier Corinne, Komuta Mina, Le Loarer François, Orbach Daniel, Rome Angélique, Minard-Colin Véronique, Brichard Bénédicte, Pluchart Claire, Thebaud Estelle, Renard Marleen, Pannier Stéphanie, Brisse Hervé, Petit Philippe, Benoist Camille, Schleiermacher Gudrun, Geoerger Birgit, Vincent-Salomon Anne, Fréneaux Paul, Pierron Gaëlle. Infantile Rhabdomyosarcomas With VGLL2 Rearrangement Are Not Always an Indolent Disease: A Study of 4 Aggressive Cases With Clinical, Pathologic, Molecular, and Radiologic Findings.. The American journal of surgical pathology. 2021. DOI: 10.1097/pas.0000000000001702.

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