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ABSTRACT
I N THIS PAPER, we describe cells from the Previously, CSF cells from Burkitt
cerebrospinal fluid (CSF) of an American lymphoma cases were described by Janota, 3
patient with Burkitt's lymphoma, with who used phase-contrast micrography.
emphasis on the technic of preparing the Others have described simple smears of
specimen. Infiltration of the central CSF, but Wright 7 found these yielded too
nervous system (CNS) is a common com- many " s m e a r cells" (unidentifiable
plication of the latter stages of Burkitt's smudges), which he believed to be rem-
lymphoma 8 with concomitant symptoms nants of Burkitt cells. He suggested the
such as paraplegia, cranial nerve palsies, addition of 20% serum to the CSF prior
or elevated intracranial pressure. 7 Thus, to centrifugation, before smearing the
proper cytology of CSF is important to deposit, in order to help keep the fragile
determine whether the cells present are Burkitt cells intact.
malignant and require cancer therapy,
or benign, perhaps indicative of infectious Methods
disease. Indeed, these patients are at
greater risk for infectious disease than Our patient was a 7-year-old white native
normal individuals. For example, Ziegler American boy, in whom the diagnosis of
and associates 8 found evidence of malig- Burkitt's lymphoma had been established
nant cells in CSF in only three of ten pa- by biopsy of an abdominal mass on April
tients who had Burkitt's lymphoma with 29, 1971. He was now referred for symp-
symptoms of paraplegia. It also should be toms of CNS disorders, etiology undeter-
noted that in all cases in which the tumor mined.
cells were found in the CSF the patients From freshly obtained CSF, uncentri-
were children of East Africa. fuged, we took two separate samples. One
was stained routinely with Wright's stain
Received December 18, 1974; accepted for pub- by the technician. The other smear was
lication January 10, 1975. prepared by filtering through a "millipore"
Address reprint requests to Howard B. Fuchs, B.A.,
New York Medical College, Basic Science Building,
filter paper (0.45 (JL) and staining the disk
Box # 3 9 3 , Valhalla, N.Y. 10595. with ordinary hematoxylin and eosin.
238
August 1975 CSF CYTOLOGY IN BURKITT'S LYMPHOMA 239
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FIG. 3 (right). Cerebrospinal fluid "millipore" preparation, same specimen as above; 95% ethanol
fixation. Hematoxylin and eosin. x 1,000.
240 FUCHS AND ROSAN A.J.C.P.—Vol.64
of CSF cells from cases of Burkitt's lym- and American types of lymphoma, the
phoma and the possibility of error from virologies and perhaps even the etiologies
routine methods. We agree with Wright's of the two might not. Perhaps an intensive
suggestion of "extra precaution" for study and comparison of African and
Burkitt's lymphoma; the technologist must American CSF cytology could help to
be made aware of the need for special illuminate this problem. At least, more
technic in handling these specimens. work should be done to investigate possible
We speculate that more attention to those other differences.
morphologic details may help resolve cer-
tain problems in the analysis of CSF speci- References
mens from American patients who have
1. Herlitzker AJ, Badruddoja M, Dube VE:
Burkitt's lymphoma. For example, ac- "Clinical and pathological differences of
cording to recent findings by Pagano and * Burkitt's lymphoma. Surg Gynecol Obstet
136:81-86, 1973
associates, 6 American Burkitt's lymphoma 2. Hirshaut Y, Cohen M, Stevens DA. Serological
material showed an absence of viral DNA, differences between American and African