ArticleHuman pathology2011
Erythroblastic sarcoma presenting as bilateral ovarian masses in an infant with pure erythroid leukemia.
Article in Human pathology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 30 citations in OpenAlex.
- Identification of an NFIA::CBFA2T3 fusion in cerebrospinal fluid confirms the diagnosis of pediatric CNS myeloid sarcoma with erythroid differentiation: a case report and literature review.Frontiers in oncology · 2026Article
- TheFrontiers in oncology · 2026Article
- Autopsy findings of acute erythroid leukemia.Autopsy & case reports · 2023Article
- Erythroblastic sarcoma in the thoracic cavity of a cow.The Journal of veterinary medical science · 2019Article
- Myeloid Sarcoma Presented as Generalized Lymphadenopathy: Mimicking Malignant Lymphoma.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2018Article
- A Rare Case of Pure Erythroid Sarcoma in a Pediatric Patient: Case Report and Literature Review.Children (Basel, Switzerland) · 2017Article
- Congenital immature pure erythroid leukemia with E-cadherin expression.International journal of hematology · 2017Article
- Myeloid sarcomas: a clinicopathologic study of 20 cases.Turkish journal of haematology : official journal of Turkish Society of Haematology · 2015Article
- Isolated Granulocytic Sarcoma of the Breast after Allogeneic Stem Cell Transplantation: A Rare Involvement Also Detected by 18FDG-PET/CT.Turkish journal of haematology : official journal of Turkish Society of Haematology · 2014Article
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Authors and funding
6 authors at 4 institutions in 1 country.
Funding
Abstract
Pure erythroid leukemia is a rare subtype of acute erythroid leukemia that is characterized by a predominant erythroid population, and erythroblastic sarcoma has not yet been described in the English literature. Here, we report a first case of erythroblastic sarcoma that presented as bilateral ovarian masses in a 3 ½-month-old infant girl with pure erythroid leukemia. Bone marrow aspirate and biopsy showed that the marrow was completely replaced by large-sized blasts consistent with erythroblasts. Immunophenotypically, both the tumor cells from the ovarian mass and bone marrow blasts were positive for CD117, glycophorin A, and hemoglobin A, demonstrating erythroid differentiation. Reverse transcriptase polymerase chain reaction showed that the tumor cells from ovarian mass expressed hemoglobin F and α1 spectrin, confirming their erythroid lineage. Conventional karyotype of the bone marrow aspirates revealed del(6)(q23q25) and trisomy 7 in all 21 cells examined. Fluorescence in situ hybridization of the ovarian mass demonstrated loss of c-myeloblastosis viral oncogene (C-MYB) at 6q23 locus in 41% of the cells, and deletion of chromosome 7 and 7q in 37% and 66% of cells, respectively. Taken together, we showed, for the first time, that pure erythroid leukemia presented as a myeloid sarcoma in the form of ovarian masses.
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