Granulocytic sarcoma, also called chloroma or myeloblastoma, is an extramedullary invasive tumor composed of neoplastic myeloid cells. In this report, we describe a 43-year-old male patient with a collision tumor composed of an adenocarcinoma and a granulocytic sarcoma in the stomach.
The coexistence of a granulocytic sarcoma and adenocarcinoma in the stomach has, to the best of our knowledge, not been reported in the literature. The diagnosis of granulocytic sarcoma is very difficult; especially in the absence of concurrent hematologic disease or in the uncommon setting of coexistence with another tumor. Cautious observation is needed when a finding of unusual atypical cells admixed with an adenocarcinoma in the stomach is confronted.
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Leukemia in gastrointestinal organs as cause of treatment failure: 378 cases analyzed Isabel Cunningham, Daniel Worthley American Journal of Hematology.2018; 93(11): 1327. CrossRef
One cancer destroys another: short report of a myeloid sarcoma causing ischaemic necrosis of an adenocarcinoma D Tucker, P Sarsfield, I Chandler, P Kerr Journal of Clinical Pathology.2014; 67(1): 70. CrossRef
Concurrence of adenocarcinoma and neuroendocrine carcinoma in the gastrointestinal tract has rarely been observed. We report two cases of gastric collision tumors (adenocarcinoma and neuroendocrine carcinoma) that developed in a 64-year-old man and a 71-year-old man. In both cases, there was a single ulcerative lesion in the stomach.
Histologically, the gastric lesions were composed of two discrete lesions: tubular adenocarcinoma at the edge of an ulcer and neuroendocrine carcinoma in the ulcer base. We will discuss collision and composite tumors.
This is to report a case of collision tumor of the urinary bladder, which was composed of papillary transitional cell carcinoma(PTCC) and osteosarcoma. Grossly the tumor was located at left antero-lateral wall and was a fungating, gray yellow, bony hard mass with papillary configuration of the luminal surface. Histologically the tumor was composed of PTCC confined to the mucosa and sarcomatous component not intermixed with the overlying PTCC. The sarcomatous area had features of classic osteosarcoma with anaplastic tumor cells and haphazardly arranged osteoid matrix, and was positive for osteonectin but entirely negative for cytokeratin or epithelial membrane antigen. Ultrastructural study demonstrated the tumor cells to be osteoblast which had rich rERs and a few lipid vesicles in plump cytoplasm without any evidence of epithelial ongin. The case is thought to be an example of collision tumor because there was no evidence of transition between PTCC and osteosarcoma.