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Shwachman-Diamond syndrome and solid tumors: Three new patients from the French Registry for Severe Chronic Neutropenia and literature review.
Bou Mitri, Fares; Beaupain, Blandine; Flejou, Jean-François; Patient, Matthieu; Okhremchuck, Ilona; Blaise, Didier; Izadifar-Legrand, Faézeh; Martignoles, Jean Alain; Delhommeau, François; Bellanne-Chantelot, Christine; Emile, Jean-François; Donadieu, Jean.
Afiliação
  • Bou Mitri F; Centre de Recherche Saint-Antoine, APHP, Armand-Trousseau Hospital, French Registry for Severe Chronic Neutropenia, CRMR of Chronic Neutropenia, Department of Pediatrics Hematology and Oncology, Sorbonne Université, Inserm, Paris, France.
  • Beaupain B; Centre de Recherche Saint-Antoine, APHP, Armand-Trousseau Hospital, French Registry for Severe Chronic Neutropenia, CRMR of Chronic Neutropenia, Department of Pediatrics Hematology and Oncology, Sorbonne Université, Inserm, Paris, France.
  • Flejou JF; Department of Pathology, Saint-Antoine Hospital, APHP, Paris, France.
  • Patient M; Department of Hematology and Oncology, Hôpital d'Instruction des Armées (HIA) Sainte-Anne, Toulon, France.
  • Okhremchuck I; Department of Pathology, HIA Sainte-Anne, Toulon, France.
  • Blaise D; Department of Hematology, Paoli-Calmettes Institut, Marseille, France.
  • Izadifar-Legrand F; Department of Hematology, Paoli-Calmettes Institut, Marseille, France.
  • Martignoles JA; Inserm, Centre de Recherche Saint-Antoine, Hématologie Biologique, Hôpital Saint-Antoine, APHP, Sorbonne Université, Paris, France.
  • Delhommeau F; Inserm, Centre de Recherche Saint-Antoine, Hématologie Biologique, Hôpital Saint-Antoine, APHP, Sorbonne Université, Paris, France.
  • Bellanne-Chantelot C; Department of Genetics, Pitié-Salpêtrière Hospital, APHP, Sorbonne University, Paris, France.
  • Emile JF; Department of Pathology, Ambroise-Paré Hospital, APHP, Boulogne, France.
  • Donadieu J; Centre de Recherche Saint-Antoine, APHP, Armand-Trousseau Hospital, French Registry for Severe Chronic Neutropenia, CRMR of Chronic Neutropenia, Department of Pediatrics Hematology and Oncology, Sorbonne Université, Inserm, Paris, France.
Pediatr Blood Cancer ; 68(7): e29071, 2021 07.
Article em En | MEDLINE | ID: mdl-33871916
ABSTRACT
Shwachman-Diamond syndrome with Shwachman-Bodian-Diamond syndrome (SBDS) biallelic variants is a rare disorder that predisposes the carrier to malignant hemopathies but solid-cancer predisposition is poorly known. Among 155 cases entered in the French Registry for Severe Chronic Neutropenia, three were identified with malignant solid tumors (ovary, breast, and esophagus). All cancers occurred during the fifth decade and, despite being localized at diagnosis, were rapidly fatal thereafter. No cancer was observed post transplantation in the 14 HSCT survivors. Based on the literature and our patient data, we can merely advance that this complication is predominantly diagnosed in adults.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Shwachman-Diamond / Neoplasias / Neutropenia Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Shwachman-Diamond / Neoplasias / Neutropenia Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article