Systemic mast cell disease associated with primary ovarian mixed malignant germ cell tumor.
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Summary
A 12-year-old girl with a mixed malignant germ cell tumor of the ovary, treated by surgery and chemotherapy, developed systemic mast cell disease (SMCD) approximately 3 months after chemotherapy.
- Type
- article
- Published
- 1998-12-01
- Cited by
- 19
- References
- 13
- OpenAlex
- https://openalex.org/W1965902756
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:11812118
Keywords
Mast cell, Germ cell, Chemotherapy, Ovary, Germ cell tumors
References
- The clonal nature of mediastinal germ cell tumors and acute myelogenous leukemia. A case report and review of the literature.
- A point mutation in the catalytic domain of c-kit induces growth factor independence, tumorigenicity, and differentiation of mast cells.
- Stepwise requirement of c-kit tyrosine kinase in mouse ovarian follicle development.
- Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles.
- Systemic Mast Cell Disease: ANALYSIS OF 58 CASES AND LITERATURE REVIEW
- Association between mediastinal germ cell tumors and hematologic malignancies: Report of two cases and review of the literature
- Systemic mast cell disease associated with primary mediastinal germ cell tumor.
- Systemic mastocytosis following mediastinal germ cell tumor: an association confirmed.
- Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder.
- Acute nonlymphocytic leukemia, preleukemia, and acute myeloproliferative syndrome secondary to treatment of other malignant diseases. II. Bone marrow cytology, cytogenetics, results of HLA typing, response to antileukemic chemotherapy, and survival in a total series of 55 patients
- Somatic c-KIT activating mutation in urticaria pigmentosa and aggressive mastocytosis: establishment of clonality in a human mast cell neoplasm
- Recombinant human stem cell factor (kit ligand) promotes human mast cell and melanocyte hyperplasia and functional activation in vivo
- W mutant mice with mild or severe developmental defects contain distinct point mutations in the kinase domain of the c-kit receptor.
Cited by
- Mastocitose cutanea e tumor de celulas germinativas: uma rara associacao
- Paediatric mastocytosis: a systematic review of 1747 cases
- Hematologic malignancies associated with germ cell tumors
- Cutaneous mastocytosis associated with a mixed germ cell tumour of the ovary: report of a case and review of the literature
- Mastocytosis in Childhood
- Tumor-intrinsic and -extrinsic roles of c-Kit: mast cells as the primary off-target of tyrosine kinase inhibitors
- Transdifferentiation and nuclear reprogramming in hematopoietic development and neoplasia
- Aggressive systemic mastocytosis after germ cell tumor of the ovary: C-KIT mutation documentation in both disease states.
- Ovarian fibrosarcoma producing multiple cytokines
- Aggressive Systemic Mastocytosis Following Ovarian Germ Cell Tumor
- Treatment of systemic mast cell disorders.
- Mast cell disease and malignant germ cell tumors.
- Progressive Hautveränderung bei einem Säugling
- A variant c‐KIT mutation, D816H, fundamental to the sequential development of an ovarian mixed germ cell tumor and systemic mastocytosis with chronic myelomonocytic leukemia
- An aggressive systemic mastocytosis preceded by ovarian dysgerminoma
- Ovarian germ cell tumor/mastocytosis with KIT mutation: A unique clinicopathological entity
- A Review of the Clinical Features and Management of Systemic Congenital Mastocytosis through the Presentation of An Unusual Prenatal-Onset Case
- Reply
- Additional file 4 of An aggressive systemic mastocytosis preceded by ovarian dysgerminoma
- Ovarian germ cell tumors
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