1Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China.
2Department of Neurology, Xijing Hospital, the Fourth Military Medical University, Xi’an 710032, Shaanxi, China.
Correspondence Address: Prof. Hong-Zhi Guan, Department of Neurology, Peking Union Meidical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China. E-mail: firstname.lastname@example.org ; Prof. Gang Zhao, Department of Neurology, Xijing Hospital, the Fourth Military Medical University, Xi’an 710032, Shaanxi, China. E-mail: email@example.com
© The Author(s) 2018. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
Cerebrospinal fluid (CSF) cytology is a fundamental test for the diagnosis of central nervous system (CNS) disease in neurological practice in China. CSF cytology provides diagnostic evidence in cases suspected of CNS infectious diseases, autoimmune encephalitis and CNS neoplastic disorders. Immunocytochemistry and flow cytometry make the cytological diagnosis more sensitive and specific. However, the diagnostic significance of CSF cytology should be interpreted and evaluated in the context of specific clinical backgrounds. Although molecular diagnostic techniques, including polymerase chain reaction and next-generation sequencing, are increasingly applied to CSF examination, the classical CSF cytology still has its horizon in the era of precision neurology and should be recommended as a routine test for CSF analysis.
Cerebrospinal fluid, cytology, neurology, infection, autoimmune
Analysis of cerebrospinal fluid (CSF) became possible with the introduction of lumbar puncture (LP) for clinical application at the beginning of the 20th century. Initial reports in the diagnostic utility of LP mainly focused on diagnosis of central nervous system (CNS) infectious disease, particularly neurosyphilis. Two reports published in 1904 describing findings of CNS tumors in CSF were seen as the beginning of CSF cytology. One was by Dufour, a French physician; the other by Walter Rindfleisch, a German physician. However the CSF cytology wasn’t fully developed until the invention of CSF concentration techniques in the 1950s by the neurologist Sayk (1923-2005), a neurologist from East Germany. He developed Sayk’s cell sedimentation chamber which was modified later and is still used in some labs in China.
CSF cytology in China mainland dates back to the 1960s and 1970s when famous Chinese neurologists, including Hou et al., Su et al., introduced the technique to major neurological centers in China. These pioneers’ contribution laid the foundation of clinical CSF research in China mainland. The CSF Cytology Society was founded in 1991 as a division of the Chinese Society of Neurology, which later was renamed as the Neuroinfection and CSF Cytology Society under suggestions of its current chairman, Dr. Gang Zhao. Currently, many neurologists read slides and sign CSF cytology reports under the certification of the Chinese Society of Neurology. The historic background of CSF cytology in China made CSF cytology a well-accepted diagnostic method in our neurological practice.
A series of conferences and educational activities was organized by the society to ensure the diagnostic quality of different CSF cytology labs around China. Neurologists in China also modified techniques for CSF cytology based on Sayk’s method and the cytocentrifuge technique. In the CSF cytology lab of the Department of Neurology in Peking Union Medical College Hospital (PUMCH), slides are prepared with the cell sedimentation technique with the Hou’s cell sedimentation chamber modified from the Sayk’s method of spontaneous cell sedimentation technique [Figure 1]. We put 0.5 mL cerebrospinal fluid into the chamber and store overnight at 4 ℃, allowing the cells to precipitate onto the slides. The slides are then air-dried and stained with May-Grunwald-Giemsa stain (MGG) and immunocytochemistry. Chinese ink stain (also called India ink stain) is used if Cryptococcus is suspected on MGG stain. Presently, over 8000 samples of CSF cytology are handled annually with this technique in the Department of Neurology in PUMCH. In contrast, in the CSF cytology lab of the Department of Neurology in Xijing Hospital, slides are prepared with the cytocentrifuge technique with a series of equipment developed and modified by Dr. Xiu-Chu Su and his colleagues. Nearly 10,000 samples of CSF cytology are handled in the Xijing Hospital annually with various type of staining methods, including modified modified Ziehl-Neelsen stain. The modified Ziehl-Neelsen stain, introduced to CSF cytology by Dr. Gang Zhao and his team, is more sensitive than the conventional Ziehl-Neelsen stain and is available in many CSF cytology labs in China. Finally, in the Department of Neurology in the Second Hospital of Hebei Medical University, Dr. Jun-Ying He and her team are now focusing their research on the diagnosis and treatment of meningeal malignancy and around 5000 samples of CSF cytology are handled annually in their lab.
Figure 1. (A) The Hou's chamber modified from the Sayk's method which is still in use in some CSF labs in China; (B) the cytocentrifuge equipment for the Su's Centrifugal method (photo provided by Yi-Ning Yang from Xijing Hospital); (C) the chambers used in the Su's Centrifugal method (photo provided by Yi-Ning Yang)
Based on various preparation and staining techniques, CSF cytology has become a fundamental test for the diagnosis of CNS disease in neurological practice in China. CSF cytology is a quantitative or semi-quantitative cytology method, which also emphasizes inflammatory findings and differential diagnoses (infectious or non-infectious etiology) beyond that of malignancy identification.
Inflammatory disorders, either infectious or autoimmune diseases of the CNS, usually induce significant changes in the cellular content of the CSF.
Types of infection involving CNS include bacterial, viral, mycotic (fungi), parasite and prion infections. Specific infectious organisms identified by CSF cytology include Cryptococcus, Toxoplasma and various species of bacteriac. Cryptococcus is the most common infectious agent observed by CSF cytology [Figure 2]; however, this kind of specific pathogenic findings only account for a small percentage of all cytology diagnoses.
Figure 2. CSF cytology prepared with cell sedimentation chamber. (A) Cryptococcusgatti with Chinese ink staining, ×100; (B) Cryptococcusgatti with Chinese ink staining, ×400; (C) eosinophil pleocytosis in CSF of a patient with Angiostrongylus cantonesis, MGG staining, ×200; (D) lymphoma cells in CSF from a patient with PCNSL, MGG staining, ×200; (E) CD20 positive lymphoma cells in CSF, immunocytochemistry, ×200; (F) Ki-67 index: 60%, immunocytochemistry, ×200. CSF: cerebrospinal fluid; MGG: May-Grunwald-Giemsa; PCNSL: primary central nervous system lymphoma
Nearly all types of CNS infections (except prion disease) have CSF cytological changes that may provide diagnostic clues of etiology. Acute bacterial infections usually induce neutrophil pleocytosis in CSF. Later on these infections also show lymphocytic pleocytosis. Acute tuberculous meningitis may also be characterized by neutrophil pleocytosis or a mixed cellular response with neutrophils and lymphocytes. In later stages of tuberculous meningitis, lymphocytic inflammation predominates while neutrophils remain present until ful clinical remission. The cytological picture of CNS viral infection predominantly shows a lymphocytic response. However, neutrophil pleocytosis may present in necrotizing cerebral processes of acute viral infections (e.g. herpes simplex virus-1 encephalitis or CNS vasculitis). Eosinophilic pleocytosis in the CSF is a hint at a parasitic infection, such as neurocysticercosis, a relatively common type of parasitic infection in North China. A cytological picture of eosinophil predominance in CSF, so called “eosinophilic meningitis”, indicates either a special type of neurocysticercosis (e.g. meningeal type of cysticercosis) or Angiostrongylus cantonesis, mostly in Southeastern China [Figure 2].
The presence of plasma cells, the antibody-synthetic cells transformed from B-lymphocyte, in CSF indicates a chronic infection (e.g. tuberculosis, syphilis or borreliosis) or intrathecal humoral immunological response. Some infections lead to a higher content of atypical lymphoid or lymphoblastic cells in the CSF, which makes the differential diagnosis from lymphoma very difficult.
Autoimmune CNS disorders include primary neuroimmune disorders [e.g. multiple sclerosis (MS), neuromyelitis optica spectrum disorders (NMOSD) and autoimmune encephalitis] and those secondary to systemic autoimmune disease.
Inflammatory reactions in CSF are observed in about half of AQP4-IgG positive NMOSD patients. The main inflammatory type is lymphocytic inflammation, while neutrophils and eosinophils are also seen in a few patients. Activated lymphocytes, activated mononuclear cells, and plasma cells can be detected in some patients’ CSF. The positive rate of the specific oligoclonal bands in AQP4-IgG positive NMOSD is lower than that in multiple sclerosis. These CSF characteristics may contribute to the diagnosis of NMOSD. A mildly increased percentage of eosinophils is common in autoimmune CNS demyelination including NMOSD, acute disseminated encephalomyelitis and transverse myelitis. The demonstration of plasma cells in CSF of patients with MS is significantly correlated with pleocytosis and intrathecal IgG synthesis.
Anti-NMDAR encephalitis is a major type of autoimmune encephalitis associated with autoantibodies against neuronal surface proteins. Intrathecal synthesis of autoantibodies is a pathological mechanism of this disease. CSF cytology findings include lymphacytic inflammation, occasionally with a mild increased percentage of neutrophils. Plasma cells are common in CSF of anti-NMDAR encephalitis which indicates intrathecal immunoglobulin synthesis. For other type of autoimmune encephalitis without the mechanism of intrathecal immunoglobulin synthesis (e.g. anti-LGI1 encephalitis and anti-GABAbR encephalitis), the CSF cytology findings are normal or less reactive.
Neuro-Behçet Syndrome (NBS) may present with various clinical manifestations. The most common neuroimaging finding is CNS midline structure involvement including brainstem, basal ganglion and thalamus. The CSF cytological findings, typically the presence of neutrophils, indicate the nature of neutrophilic vasculitic of NBS and are important clues in the diagnosis of NBS.
Neuropsychiatric systemic lupus erythematosus (SLE) is the CNS involvement of SLE. According to our observation, he CSF cytology was abnormal in 32.9% of SLE patients, which showed lymphocytic inflammatory reactions or lymphocyte - neutrophil inflammation. Among these cases with positive CSF cytological findings, activated lymphocytes, plasma cells and activated monocytes were frequently present. Abnormal endocytosis of monocytes, which presented as monocytes phagocytosing lymphocytes or plasma cells, was shown in some cases.
CSF cytology findings in CNS inflammatory disease are relatively non-specific. However, when we consider the cytological findings under the clinical background of an individual patient, then the so-called “clinical-CSF cytological syndrome” can lead to a specific diagnosis [Table 1]. For example, in patients with recurrent CNS midline structure involvement and neutrophil pleocytosis or a mixed cellular response of CSF cytology, Neuro-Behçet disease should be highly suspected.
CSF cytological syndrome with etiological indication
|CSF cytology||Clinical syndrome||Etiological consideration|
|Lymphatic inflammation||Acute encephalitis||Viral encephalitis|
|Lymphatic inflammation||Acute mild or moderated meningism||Viral meningitis|
|Lymphatic inflammation||Shepherd with chronic meningitis or chronic encephalomyelitis||Neurobucellosis|
|Mixed reaction with lymphocyte and neutrophil||Recurrent brain-stem encephalitis or diencephalitis||Neuro-Behçet disease|
|Mixed reaction with lymphocytes and neutrophils||Chronic or subacute encephalitis||Tubercular meningitis|
|Mixed reaction with Lymphocytes, eosinophils and plasma cells||Chronic meningitis||Neurocysticercosis|
|Eosinophilic inflammatory||Acute meningitis in patients from Southeastern China||Angiostrongylus cantonesis|
|Lymphatic inflammation with mild increased eosinophils||Acute encephalomyelitis or myelitis||Transverse myelitis|
Identification of tumor cells by CSF cytology is direct and specific evidence of leptomeningeal involvement by neoplasms. The appearance of malignant cells in CSF usually indicates generalized seeding of the leptomeninges by tumor cells. The prevalence of leptomeningeal involvement of different tumors is important to the cytologists and clinicians to make an accurate clinical-cytoloical conclusion. According to Prayson and Fischler, the most commonly identified malignancy in CSF specimens in adults is metastatic neoplasms. Primary central nervous system neoplasms (e.g. medulloblastoma) account for a higher percentage of CSF specimens in the pediatric population than in the adult population. We reviewed CSF cytology results from PUMCH between 1984 and 2003, including 3922 specimens. Forty-nine cases (1.25%) were positive for malignant cells. Diagnoses included metastatic tumors (26 cases), metastatic lymphoma/leukemia (7 cases), primary CNS neoplasms (10 cases) and malignant unclassified neoplasms (6 cases).
Cytology deals with single cells without histological architecture, so cytologists often face the challenge of arriving at a definitive final diagnosis. Immunocytochemistry and immunophenotyping by flow cytometry are helpful for CSF cytology. For example, it was estimated that CSF cytology combined with immunocytochemistry could indicate diagnostic findings in 50% of cases with primary central nervous system lymphoma (PCNSL). Flow cytometric analysis (FCA) and polymerase chain reaction (PCR) of rearranged IgH and TCR genes of CSF are widely used in the diagnosis of PCNSL[16,17]. To study the diagnostic value of CSF cytology in the diagnosis of PCNSL, we retrospectively analyzed the data of 21 patients of PCNSL with positive CSF cytological findings. Conventional CSF cytology, immunocytochemistry, flow cytometric analysis and PCR of rearranged IgH and TCR genes of CSF were performed. The clinical and neuroimaging types of 21 patients included meningeal type (n = 13), parenchymal type (n = 4), ependymal type (n = 3), and optic type (n = 1). The CSF of all the 21 patients had atypical lymphocytes, suggestive of lymphoma. Of the 20 cases in which immunocytochemistry was performed, 17 showed B-lymphocyte predominance, which was consistent with the diagnosis of B cell lymphoma. FCA of 7 cases showed a significant increase in the percentage of B cells in 5 patients, indicating B cell lymphoma, and NK/T-lymphocyte predominance in 1 case, indicating an NK/T lymphoma. On analysis of the IgH and TCR genes in CSF of 4 patients, IgH monoclonal was found in 3 cases and TCR monoclonal in 1 case [Figure 2]. In fact, PCNSL is now one of the most common primary CNS neoplasms identified by comprehensive CSF cytological studies.
The application of molecular diagnostic techniques, including polymerase chain reaction and next-generation sequencing in CSF studies is booming in an era of precision medicine[19,20]. These novel techniques may be used to diagnose neoplastic meningopathy without cytological evidence[19,20]. However a final diagnosis based only on molecular techniques without morphological or cytological evidence should be avoided in clinical practice in order to prevent risks of over-diagnosis and misdiagnosis. CSF cytology is still the cornerstone of neurological diagnosis. The classical CSF examinations, including CSF cytology, still has their horizon in the era of precision neurology.
The authors thank Yi-Ning Yang, Guo-Dong Feng, Jun-Ying He, Hui Bu and Yue-Li Zou for their correspondence on the information of their CSF lab.Authors’ contributions
Both authors drafted the manuscript, read and approved the final manuscript.Financial support and sponsorship
None.Conflicts of interest
There are no conflicts of interest.Patient consent
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© The Author(s) 2018.
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