scholarly journals Bilateral osteoporotic bone marrow defects of the mandible: a case report

2012 ◽  
Vol 8 (1) ◽  
Author(s):  
Diego Mauricio Bravo-Calderón ◽  
Denise Tostes Oliveira ◽  
Wagner Humberto Martins dos Santos
Author(s):  
NATHALIA DE ALMEIDA FREIRE ◽  
TUANNY LIMA RANGEL ◽  
AMANDA DE SOUZA SANT'ANNA ◽  
RAPHAELA CAPELLA ◽  
SARAH ANTERO ◽  
...  

Author(s):  
Natália Galvão Garcia ◽  
Francisco Barbara Abreu Barros ◽  
Márcia Maria Dalmolin Carvalho ◽  
Denise Tostes Oliveira

Author(s):  
José Augusto Santos Silva ◽  
Paulo Ricardo Saquete Martins Filho ◽  
Maria do Carmo Correia ◽  
Raquel Correia de Medeiros ◽  
Marta Rabello Piva

2020 ◽  
Vol 1 (2) ◽  
Author(s):  
Abbas Al-Ramzi ◽  
Maysoun Kasem ◽  
Karim Ahmed

 BACKGROUND: Osteoporotic bone marrow defect of the jaw is an uncommon localized radiolucency that consists of hematopoietic red marrow with varying amounts of fatty yellow marrow. The lesion is usually asymptomatic and accidentally discovered during a routine radiographic examination; however, some studies showed different results. CASE REPORT: This is an uncommon case of bilateral mandibular osteoporotic bone marrow defect in a 40-year- old healthy female. One of the defects reoccurred, and it involves dental implants. PLAN OF TREATMENT: Lesion was managed by curettage and the patient was followed up after 1,6,12 months. CONCLUSIONS: in order to diagnose FOBMD and differentiate it from other lesions, further researches are needed to help fully understand it, since the exact incident and etiology are not established yet. 


2021 ◽  
Author(s):  
Kenta Yoshida ◽  
Takao Oyama ◽  
Takenori Takahata ◽  
Sae Kudo ◽  
Yuki Sato ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-3
Author(s):  
Samin Alavi ◽  
Maryam Ebadi ◽  
Alireza Jenabzadeh ◽  
M. T. Arzanian ◽  
Sh. Shamsian

Herein, the first case of childhood erythrophagocytosis following chemotherapy for erythroleukemia in a child with monosomy 7 is reported. A 5-year-old boy presented with anemia, thrombocytopenia, and hepatosplenomegaly in whom erythroleukemia was diagnosed. Prolonged pancytopenia accompanied by persistent fever and huge splenomegaly and hepatomegaly became evident after 2 courses of chemotherapy. On bone marrow aspiration, macrophages phagocytosing erythroid precursors were observed and the diagnosis of HLH was established; additionally, monosomy 7 was detected on bone marrow cytogenetic examination. In conclusion, monosomy 7 can lead to erythrophagocytosis associated with erythroid leukemia and should be considered among the chromosomal abnormalities contributing to the association.


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