2022
DOI: 10.1182/blood.2022018036
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Metastatic angiosarcoma in a bone marrow biopsy

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Cited by 3 publications
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“…Among mesenchymal tumors, Ewing sarcoma and pediatric rhabdomyosarcoma BMI is not uncommon [24][25]; more rarely, bone marrow infiltration from other histologic subtypes like angiosarcoma [26], epithelioid sarcoma [27] and follicular dendritic cell sarcoma [28] has been reported. Given the aggressiveness of such sarcoma subtypes, most cases were treated with high dose, multidrug regimens with poor responses and severe hematological toxicity, often fatal.…”
Section: Discussionmentioning
confidence: 99%
“…Among mesenchymal tumors, Ewing sarcoma and pediatric rhabdomyosarcoma BMI is not uncommon [24][25]; more rarely, bone marrow infiltration from other histologic subtypes like angiosarcoma [26], epithelioid sarcoma [27] and follicular dendritic cell sarcoma [28] has been reported. Given the aggressiveness of such sarcoma subtypes, most cases were treated with high dose, multidrug regimens with poor responses and severe hematological toxicity, often fatal.…”
Section: Discussionmentioning
confidence: 99%
“…The prognosis of angiosarcomas is notably poor ( 19 ), with frequent occurrences of both local recurrence and distant metastasis ( 31 , 32 ), typically resulting in a reported 5-year survival rate of approximately 31–33% ( 8 , 33 ). Angiosarcoma manifesting in bone exhibits a significantly bleaker prognosis compared to general angiosarcoma, with a 5-year survival rate of 20% and an approximate median survival time of 10 months ( 34 , 35 ).…”
Section: Discussionmentioning
confidence: 99%