Detection and quantification of CSF malignant cells by the CellSearch® technology in patients with melanoma leptomeningeal metastasis

2013 ◽  
Vol 30 (2) ◽  
Author(s):  
Emilie Le Rhun ◽  
Qian Tu ◽  
Marcelo De Carvalho Bittencourt ◽  
Isabelle Farre ◽  
Laurent Mortier ◽  
...  
Lung Cancer ◽  
2015 ◽  
Vol 90 (2) ◽  
pp. 352-357 ◽  
Author(s):  
Qian Tu ◽  
Xianglei Wu ◽  
Emilie Le Rhun ◽  
Marie Blonski ◽  
Basile Wittwer ◽  
...  

2014 ◽  
Vol 16 (suppl 2) ◽  
pp. ii50-ii50
Author(s):  
M. Blonski ◽  
B. Wittwer ◽  
G. Faure ◽  
L. Simon ◽  
M. D. C. Bittencourt ◽  
...  

2021 ◽  
pp. 1248-1253
Author(s):  
Benjamin Lardinois ◽  
Laurence Miller ◽  
Adrien Randazzo ◽  
Terry Laurent ◽  
Régis Debois ◽  
...  

In the cerebrospinal fluid (CSF), the demonstration of malignant cells by cytological examination is currently the gold standard for the diagnosis of leptomeningeal carcinomatosis (LC). However, a positive cytology is observed in only 50–60% of patients with LC and highly dependent on pre-analytical factors. The hematology laboratory could provide an immediate and accurate diagnosis, but diagnostic sensitivity is not always optimized once the sample is received. We hereby report a 49-year-old woman with a 3-year grade III invasive ductal carcinoma who was admitted to the emergency department due to headaches, nausea, and vomiting. The CSF revealed pleocytosis with suspicious high fluorescent cells on the hematology analyzer concomitantly with biochemical alterations. Cytomorphological examination confirmed tumor cells, thus diagnosing a leptomeningeal metastasis of her breast cancer. The patient was eventually transferred to palliative care. Cytological examination is a valuable tool for a rapid diagnosis of LC if diagnostic performance is optimized. In addition to repeated CSF collections with a sufficient volume (5–10 mL), this could be reached by processing the CSF as soon as possible, taking into account the fluorescence information from the analyzer, proceeding systematically to microscopic examination even with normal CSF white blood cell count, and providing quality improvement of the staff to identify malignant cells.


Author(s):  
K. Brasch ◽  
J. Williams ◽  
D. Gallo ◽  
T. Lee ◽  
R. L. Ochs

Though first described in 1903 by Ramon-y-Cajal as silver-staining “accessory bodies” to nucleoli, nuclear bodies were subsequently rediscovered by electron microscopy about 30 years ago. Nuclear bodies are ubiquitous, but seem most abundant in hyperactive and malignant cells. The best studied type of nuclear body is the coiled body (CB), so termed due to characteristic morphology and content of a unique protein, p80-coilin (Fig.1). While no specific functions have as yet been assigned to CBs, they contain spliceosome snRNAs and proteins, and also the nucleolar protein fibrillarin. In addition, there is mounting evidence that CBs arise from or are generated near the nucleolus and then migrate into the nucleoplasm. This suggests that as yet undefined links may exist, between nucleolar pre-rRNA processing events and the spliceosome-associated Sm proteins in CBs.We are examining CB and nucleolar changes in three diverse model systems: (1) estrogen stimulated chick liver, (2) normal and neoplastic cells, and (3) polyploid mouse liver.


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