Microangiopathic Hemolytic Anemia as the First Manifestation of Metastatic Signet Ring Cell Carcinoma of Unknown Origin: A Case Report and Review of Literature / 대한진단검사의학회지
The Korean Journal of Laboratory Medicine
; : 157-161, 2011.
Article
in En
| WPRIM
| ID: wpr-131138
Responsible library:
WPRO
ABSTRACT
Microangiopathic hemolytic anemia (MAHA) occurs occasionally as a paraneoplastic syndrome in some solid tumors, but MAHA accompanied by signet ring cell carcinoma of an unknown origin is very rare. In this study, we present the case of an 80-yr-old man who was admitted to the hospital because of a 1-month history of lower back pain and dyspnea. He was diagnosed with MAHA on the basis of the laboratory findings that revealed anemia with schistocytes, decreased haptoglobin levels, and a negative direct Coombs' test. Bone marrow examination, which was performed because of the progression of anemia, revealed bone marrow metastases of signet ring cell carcinoma with extensive bone marrow necrosis. However, the primary origin of this signet ring cell carcinoma was not found. When the cause of progressive MAHA is unknown, the possibility of cancer-associated MAHA must be excluded by performing additional tumor workup, including the detection of tumor markers, gastric and colorectal endoscopic examinations, bone marrow examinations, and positron emission tomography-computed tomography or bone scans.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Purpura, Thrombotic Thrombocytopenic
/
Haptoglobins
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Immunohistochemistry
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Biomarkers, Tumor
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Tomography, X-Ray Computed
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Endoscopy, Gastrointestinal
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Carcinoma, Signet Ring Cell
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Bone Marrow Neoplasms
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Positron-Emission Tomography
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Necrosis
Limits:
Aged
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Aged80
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Humans
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Male
Language:
En
Journal:
The Korean Journal of Laboratory Medicine
Year:
2011
Type:
Article