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Acta Cytol ; 47(6): 1087-90, 2003.
Article in English | MEDLINE | ID: mdl-14674086

ABSTRACT

BACKGROUND: Meningeal carcinomatosis (MC) rarely occurs as the first evidence of a tumor. In such cases cytology of the cerebrospinal fluid is crucial to the diagnosis. The most frequent primary MCs are lung and breast cancers. MC from a gallbladder carcinoma is uncommon. CASE: A 58-year-old woman presented with paroxysmal headaches, seizures and coma. Analysis of the cerebrospinal fluid revealed carcinoma cells and a low protein concentration. Only postmortem examination discovered gallbladder adenocarcinoma to be the source of the tumor cells. CONCLUSION: A case with the onset of MC secondary to rare mucinous adenocarcinoma of the gallbladder is presented. Cytology of the cerebrospinal fluid was the only examination that uncovered malignancy. Nine similar cases were found in the literature. Low cerebrospinal fluid protein seems to be of diagnostic value.


Subject(s)
Adenocarcinoma/secondary , Cerebrospinal Fluid/cytology , Gallbladder Neoplasms/pathology , Meningeal Neoplasms/secondary , Meninges/pathology , Adenocarcinoma/cerebrospinal fluid , CA-19-9 Antigen/metabolism , Carcinoembryonic Antigen/metabolism , Cerebrospinal Fluid Proteins/analysis , Cerebrospinal Fluid Proteins/metabolism , Coma/etiology , Coma/pathology , Fatal Outcome , Female , Gallbladder Neoplasms/cerebrospinal fluid , Gallbladder Neoplasms/diagnostic imaging , Gliosis/etiology , Gliosis/pathology , Glucose/cerebrospinal fluid , Headache/etiology , Headache/pathology , Humans , Meningeal Neoplasms/cerebrospinal fluid , Middle Aged , Neoplasm Metastasis/pathology , Seizures/etiology , Seizures/pathology , Tomography, X-Ray Computed
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