Epidural Spinal Cord Compression in Acute Myelogenous Leukemia

1980 ◽  
Vol 37 (5) ◽  
pp. 319-319 ◽  
Author(s):  
J. Hildebrand ◽  
L. Leenaerts ◽  
Y. Nubourgh ◽  
A. Verhest ◽  
J. Flament-Durand
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Cheng-Rui Bai ◽  
Xiang Li ◽  
Jing-Shi Wang ◽  
Jin-Jun Li ◽  
Ning Liu ◽  
...  

Abstract Background Myeloid sarcoma is a rare, extramedullary, solid tumor derived from immature myeloid cell precursors. It is most frequently accompanied by acute myelogenous leukemia, though infrequently found in non-acute myelogenous leukemia patients. The tumor may involve any part of the body, but the lumbar spine is seldom involved. The present case study aims to understand the diagnosis and surgical treatment of a rare primary isolated myeloid sarcoma of the lumbar spine causing aggressive spinal cord compression in a non-acute myelogenous leukemia patient. Case presentation A 29-year-old man complained of an aggressive radiating pain to the lower extremities and moderate dysuria with a Visual Analogue Scale score that gradually increased from 3 to 8. Lumbar enhanced magnetic resonance imaging and computed tomography revealed a lumbar canal lesion at lumbar spine L2 to L4 with spinal cord compression. A whole body bone scan with fused single photon emission computed tomography/computed tomography demonstrated abnormal 99mTc-methylene diphosphonate accumulation in the L3 lamina and spinous process. No evidence of infection or hematology disease was observed in laboratory tests. Due to rapid progression of the symptoms and lack of a clear diagnosis, decompression surgery was performed immediately. During the operation, an approximately 6.0 × 2.5 × 1.2 cm monolithic, fusiform, soft mass in the epidural space and associated lesion tissues were completely resected. The radiating pain was relieved immediately and the dysuria disappeared within 1 week. Intraoperative pathological frozen section analysis revealed a hematopoietic malignant tumor and postoperative immunohistochemistry examination confirmed the diagnosis of myeloid sarcoma. Conclusions The primary isolated aggressive lumbar myeloid sarcoma is rarely seen, the specific symptoms and related medical history are unclear. Surgery and hematological treatment are effective for understanding and recognizing this rare tumor.


2020 ◽  
Vol 54 (2) ◽  
Author(s):  
Ronna Cheska V. De Leon ◽  
Camille Ariadne C. Tanchanco ◽  
Ma. Angelina L. Mirasol ◽  
Joven Jeremius Q. Tanchuco

Myeloid sarcoma, characterized by the presence of immature myeloid cells occurring at an extramedullary site, is a rare manifestation of acute myelogenous leukemia (AML). Spinal cord compression as an initial presentation of AML is very rare with only a few reported cases. We discuss a case of a 22-year-old male who presented with bicytopenia and paraplegia. Workups were consistent with AML with monocytic differentiation. Chromosomal analysis revealed loss of Y and t (8;21). Spinal cord MRI showed intradural extramedullary-enhancing soft tissue lesions at levels T2 to T7 and L5 to S1, suspected to be myeloid sarcoma. Patient, however, succumbed to severe nosocomial infection prior to initiation of chemotherapy and radiotherapy.


2020 ◽  
Vol 78 (10) ◽  
pp. 663-664
Author(s):  
Renan Ramon Souza LOPES ◽  
Larissa Soares CARDOSO ◽  
Franz ONISHI

1985 ◽  
Vol 47 (1) ◽  
pp. 3-10 ◽  
Author(s):  
Shuichi INADA ◽  
Taizo KOHNO ◽  
Iseko SAKAI ◽  
Yoriko SHIMAMOTO ◽  
Nobutaka IMAMURA ◽  
...  

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