Advances in Central Nervous System Tumor Classification.

Historically, the classification of tumors of the central nervous system (CNS) relies on the histologic appearance of cells under a microscope; however, the molecular era of medicine has resulted in new diagnostic paradigms anchored in the intrinsic biology of disease. The 2021 World Health Organization (WHO) reformulated the classification of CNS tumors to incorporate molecular parameters, in addition to histology, to define many tumor types. A contemporary classification system with integrated molecular features aims to provide an unbiased tool to define tumor subtype, the risk of tumor progression, and even the response to certain therapeutic agents. Meningiomas are heterogeneous tumors as depicted by the current 15 distinct variants defined by histology in the 2021 WHO classification, which also incorporated the first moelcular critiera for meningioma grading: homozygous loss of CDKN2A/B and TERT promoter mutation as criteria for a WHO grade 3 meningioma. The proper classification and clinical management of meningioma patients requires a multidisciplinary approach, which in addition to the information on microscopic (histology) and macroscopic (Simpson grade and imaging), should also include molecular alterations. In this chapter, we present the most up-to-date knowledge in CNS tumor classification, particularly in meningioma, in the molecular era and how it could affect their future classification and clinical management of patients with these diseases.

Supratentorial meningeal melanocytoma mimicking meningioma: case report and literature review.

Introduction: Primary melanocytic tumors originating from CNS melanocytes are rare, with a low incidence of 0.7 cases per 10 million annually. This study focuses on primary leptomeningeal melanocytomas, emphasizing their epidemiology, clinical characteristics, and diagnostic challenges. Despite their infrequency, these tumors warrant attention due to their unique features and potential for local recurrence. Case Report: A 32-year-old female presented with syncope and seizures, leading to the discovery of two left-sided supratentorial lesions initially misidentified as convexity meningiomas. Detailed imaging suggested meningioma-like features, but intraoperative findings revealed unexpected hyperpigmented lesions. Histopathological examination, supported by immunohistochemistry, confirmed primary leptomeningeal melanocytoma. The surgical approach and subsequent management are discussed. Discussion: The discussion emphasizes challenges in diagnosing primary leptomeningeal melanocytomas. Treatment debates, especially regarding adjuvant radiotherapy, are explored. Recurrence risks stress the importance of vigilant follow-up, advocating for complete surgical resection as the primary approach. The rarity of supratentorial cases adds complexity to diagnosis, necessitating a multidisciplinary approach. Insights from this case contribute to understanding and managing primary leptomeningeal melanocytomas, addressing challenges in differentiation from more common tumors and prompting ongoing research for refined diagnostics and optimized treatments. Conclusion: This study contributes insights into primary leptomeningeal melanocytomas, highlighting their rarity in supratentorial regions. The case underscores the importance of a multidisciplinary approach, incorporating clinical, radiological, and histopathological expertise for accurate diagnosis and tailored management. Ongoing research is crucial to refine treatment strategies, enhance prognostic precision, and improve outcomes for individuals with this uncommon CNS neoplasm.

Management experience of pediatric meningioma in a Mexican reference center.

OBJECTIVE: Determine the histopathological and clinical characteristics of patients diagnosed with meningiomas and to establish the frequency of these tumors in the pediatric population Mexican. Determine the NF1/2 frequency in meningioma pediatric. METHODS: Samples from the histopathology file were reviewed, and from the complete clinical file the following patient data was reviewed: age, gender, diagnosis, diagnosis year, surgical resection, location, tumor size, symptoms, and family background. The frequency of NF1/2 in pediatric meningioma was reviewed in literature. RESULTS: Forty-four de novo cases were collected from pediatric patients; 19 were female patients and 25 males. The most frequent histological subtype was transitional meningioma. Of all the cases, 75% had a supratentorial localization and 20% had an extramedullary intrarachidian localization. Some clinical manifestations included seizures, paresis, headache, and visual disturbances. CONCLUSION: There is a low incidence of meningiomas in the pediatric population, more than 70% are Grade I, and they have supratentorial localization.

Meningioma parasagital y hematoma subdural crónico, una asociación inusual / Parasagittal meningioma and chronic subdural hematoma, unusual association

RESUMEN En muchas ocasiones, los pacientes con tumores cerebrales tienen una variedad de síntomas psiquiátricos inespecíficos. Algunos de estos pueden constituir la primera o única manifestación del tumor, sin la presencia de ningún síntoma o signo neurológico. El diagnóstico ha de basarse en la anamnesis completa y en la exploración neurológica; la neuroimagen confirmará el diagnóstico clínico. Con el presente trabajo se describió la asociación inusual de hematoma subdural crónico y meningioma parasagital en un caso presentado. Se trató de un paciente de 68 años con antecedentes de esquizofrenia. Acudió a consulta con una hemiparesia izquierda. Se le realizó una tomografía axial computarizada de cráneo y arrojó un hematoma subdural crónico y un meningioma parasagital derecho. Se le aplicó tratamiento quirúrgico en dos tiempos operatorios. Su evolución posquirúrgica transcurrió sin complicaciones (AU).

ABSTRACT In many cases, patients with brain tumors have a variety of nonspecific psychiatric symptoms. Some of them can be the first or the only manifestation of the tumor, without presenting any neurological signs or symptoms. The diagnosis must be based on the complete anamnesis and on the neurological examination. The neuroimaging will confirm the clinical diagnosis. The unusual association of a chronic subdural hematoma and a parasagittal meningioma was described in a case presented in the current work. It dealt with a patient, aged 68 years with antecedents of schizophrenia. He assisted the consultation with left hemiparesis. A skull computed tomography showed a chronic subdural hematoma and a right parasagittal meningioma. He underwent a two-steps surgery. His post-surgery evolution ran without complications (AU).

Paraplegia due to spinal meningioma during the third trimester of pregnancy: case report and literature review.

INTRODUCTION: Spinal meningiomas represent 25-45% of intradural spinal tumors and ~2% of meningiomas of the central nervous system (CNS), and their occurrence during pregnancy is unusual. We present an updated literature review. CASE REPORT: A 36-year-old woman, at 32.6 weeks of gestation, was hospitalized for urinary tract infection and urinary retention. One month earlier, she had decreased strength in lower limbs, and this weakness rapidly progressed to flaccid paraplegia without sphincters control. Magnetic resonance imaging (MRI) revealed a well-defined intradural extramedullary lesion in T3-T4. Using a posterolateral approach, the tumor was completely removed; however, there was no clinical improvement, and the patient was discharged with an impairment scale (AIS) grade A. Histopathology examination indicated a psammomatous meningioma. DISCUSSION: Meningiomas are benign tumors that are slowly progressive; however, the hemodynamic and hormonal changes of pregnancy are related to their accelerated growth. Reports show that the onset of the symptoms during the third trimester of pregnancy, including early neurological symptoms or signs of spinal cord compression, can be easily attributed to those of pregnancy by both the patient and the doctor. The time to diagnosis and medulla compression time are thus prolonged, which can be further compounded in middle-high income countries due to limitations in obtaining images for evaluation. Although rare, spinal meningiomas should be considered in the differential diagnosis of patients with neurological symptoms during pregnancy. Their early recognition is important to avoid irreversible neurological damage.

Intracranial Inflammatory Myofibroblastic Tumor: A Review of 49 cases

Inflammatory Myofibroblastic Tumor (IMT) is a rare pathologic entity that was first described in 1973. This lesion is most commonly found in the lungs, but other organs' involvement has also been reported. Intracranial location of Inflammatory Myofibroblastic Tumor is rare, and the first case was reported in 1980. An intriguing fact about the intracranial IMT is its resemblance with meningioma on clinical presentation and neuroimaging. We came across a case of intracranial Inflammatory Myofibroblastic Tumor (IIMT) in a 27-year-old male who presented with recurrent episodes of seizures and was diagnosed as meningioma on neuroimaging. The lesion did not subside with medical management and kept on progressing in size. The patient had to undergo surgery, and diagnosis of Inflammatory Myofibroblastic Tumor was ascertained on histopathology. This 'surprise' diagnosis prompted us to review the literature on all cases of IIMTs reported to date to better understand the entity and its implications. In this review article, we present our observations regarding various studied parameters, including patient profile, clinical presentation, site of involvement, focality of the lesion, special associations, and lines of management of the 49 published cases of IIMTs.

Association between intracranial aneurysm and meningiomas: An integrative survival Analysis with identification of prognostic factors.

OBJECTIVE: To analyze prognostic factors in clinical association between intracranial aneurysm (IA) and meningioma. Prognostic factors on overall survival (OS) were evaluated. METHODS: We selected articles, published from January 1944 to December 2018 on the Medical databases (Web of Sciences, Medline and EMBASE) and included case series and reports. Clinical information was obtained and variables associated with the primary outcome of 27-mo survival were identified through Cox regression models. RESULTS: The study evaluated 77 patients. Female represented 76.6 % (n = 59), a ratio of 3.27 female: 1 male. The age range was 7-84 years old, with an average of 54.74 (SD: 14.30). Age and sex were not significant statistically different between the two groups for overall survival (OS) (log-rank P = 0.806), (log-rank P = 0.983) respectively. 77.9 % (n = 60) were ipsilateral, the same side was 4 times more common in univariate analysis (P = 0.052; 95 % CI, 0.924-17.319). Most aneurysms were detected in the internal carotid artery, 29.87 %. In Clinical data, 62.33 % (n = 48) had exclusive tumor symptoms, while 25.97 % (n = 20) presented exclusively subarachnoid hemorrhage (SAH). In multivariate analysis, although there is an independent protective factor for those who did not have SAH (HR; 0.099; CI; 0.010-0.986; P = 0.049) and the treatment is an independent predictor for OS (HR, 42.096; CI, 4.270-415.056; P = 0.01). CONCLUSION: This is the first study to approach this association. This is not just an occasional finding, but it seems to have a shared pathophysiology. Unruptured aneurysms and treatment modality were protective independent factors for OS. Prospective studies are warranted to provide definitive answers.

Proteomics pinpoints alterations in grade I meningiomas of male versus female patients.

Meningiomas are among the most common primary tumors of the central nervous system (CNS) and originate from the arachnoid or meningothelial cells of the meninges. Surgery is the first option of treatment, but depending on the location and invasion patterns, complete removal of the tumor is not always feasible. Reports indicate many differences in meningiomas from male versus female patients; for example, incidence is higher in females, whereas males usually develop the malignant and more aggressive type. With this as motivation, we used shotgun proteomics to compare the proteomic profile of grade I meningioma biopsies of male and female patients. Our results listed several differentially abundant proteins between the two groups; some examples are S100-A4 and proteins involved in RNA splicing events. For males, we identified enriched pathways for cell-matrix organization and for females, pathways related to RNA transporting and processing. We believe our findings contribute to the understanding of the molecular differences between grade I meningiomas of female and male patients.

Neurofibromatosis tipo 2, entidad a tener presente durante la práctica clínica / Neurofibromatosis type 2, entity to have present during clinical practice

La neurofibromatosis tipo 2 es un trastorno poco frecuente, que pertenece al grupo de las neurofibromatosis, que se caracterizan por la mayor propensión al desarrollo de tumores. Se presenta con múltiples tumores no malignos del sistema nervioso, incluidos schwannomas, meningiomas, ependimomas y gliomas, siendo los schwannomas vestibulares bilaterales una característica clásica. La mayoría de los casos se diagnostican en la adultez, sin embargo, las características clínicas habitualmente están presentes durante muchos años antes del diagnóstico. Es importante un alto índice de sospecha y un adecuado examen cutáneo y neurológico, ya que es crítico para hacer un diagnóstico correcto y precoz, y así, realizar un tratamiento interdisciplinario adecuado, evitando posibles complicaciones como son la pérdida auditiva y el uso de ayudas técnicas.

Neurofibromatosis type 2 is a rare disorder, belonging to the group of neurofibromatosis, which are characterized by the propensity for tumor development. The usual presentation are multiple non-malignant tumors of the nervous system, including schwannomas, meningiomas, ependymomas, and gliomas, with bilateral vestibular schwannomas being a classic feature. Most cases are diagnosed in adulthood; however, the clinical features are usually present for many years before diagnosis. A high index of suspicion and an adequate skin and neurological examination are important, since it is critical to make a correct and early diagnosis, so an appropriate interdisciplinary treatment can be performed, avoiding possible complications such as hearing loss and use of technical aids.

Meningiomas intracraneales. Experiencia de dos años en el servicio Neurocirugía de Matanzas / Intracranial meningiomas. Two-year experience in the service Neurosurgery of Matanzas

RESUMEN Introducción: los meningiomas constituyen la segunda causa de tumores cerebrales primarios, en el adulto. Representan hasta el 32 % del total de los mismos. Objetivo: describir el comportamiento del meningioma intracraneal en los pacientes investigados. Materiales y métodos: se realizó un estudio analítico, descriptivo, retrospectivo a los pacientes neurointervenidos con meningioma intracraneal, en el Servicio de Neurocirugía del Hospital Docente Universitario "Comandante Faustino Pérez Hernández", de la provincia Matanzas. En el período comprendido entre el 1ero de enero de 2017 al 1ero de enero del 2019. Los 15 pacientes intervenidos conformaron el universo de estudio. Resultados: la media poblacional fue de 55 años. Predominó el sexo femenino en un 73,3 %. La cefalea fue la manifestación clínica más frecuente, igualmente, que los meningiomas de la convexidad cerebral. En cuanto a la topografía, la media del tamaño de la lesión fue de 4,4 cm. La variedad meningotelial (40 %) fue la que predominó. El grado II de resección fue el que más se empleó. El edema cerebral postquirúrgico predominó en un 26,6 %. La puntuación de la escala de Karnofsky al egreso fue superior que al ingreso. Conclusiones: cuanto más precoz se realice el diagnóstico clínico y tratamiento quirúrgico en los pacientes portadores de meningioma, mejor será su calidad de vida al egreso (AU).

ABSTRACT Introduction: meningiomas are the second cause of primary brain tumors in adults, representing up to 32 % of the total. Objective: to describe the behavior of intracranial meningioma in the studied patients. Materials and methods: a retrospective, descriptive, analytical study was conducted on neurosurgery patients with intracranial meningioma in the Neurosurgery service of the University Teaching Hospital "Comandante Faustino Pérez Hernández" of the province of Matanzas, in the period from January 1st 2017 to January 1st, 2019. The 15 patients undergoing neurosurgery were the study universe. Results: the population mean was 55 years; female sex prevailed (73.3 %). Headache was the most frequent clinical manifestation as well as meningiomas of cerebral convexity in terms of topography. The average lesion size was 4.4 cm; the meningothelial variety (40 %) was the most commonly found; grade II resection was the most used one. Post-surgical cerebral edema (26.6%) predominated. Karnofsky scale score at discharge was higher than at admission. Conclusions: the earlier the clinical diagnosis and surgical treatment are performed in patients with meningioma the better will be their quality of life at discharge (AU).

Meningioma de nervio óptico y seno cavernoso: Reporte de caso / Optic nerve and cavernous sinus meningiomas: case report

Los meningiomas de nervio óptico y de seno cavernoso son patologías poco frecuentes, y hasta el momento no ha habido ningún reporte de que se presenten ambos en un mismo paciente. Cabe resaltar que cuando llega un paciente a consulta diagnosticado con alguna patología, asumimos que este diagnóstico es adecuado y pertinente. Pero en nuestro caso, el paciente presentó signos y síntomas de etiología desconocida que hicieron que se re-evaluarán los diagnósticos oftalmológicos que traía la paciente, encontrando que había sido tratada por un diagnóstico que no le correspondía y a su vez este hallazgo nos ayudó a encontrar la verdadera causa(AU)

Optic nerve and cavernous sinus meningiomas are uncommon pathologies, and so far there have not been previously reported to occur in the same patient. It should be emphasized that when a patient arrives at a doctor's office diagnosed with pathology, we assume that this diagnosis is appropriate and pertinent. But in our case, the patient presented signs and symptoms of unknown etiology that led to a re-evaluation of the previous ophthalmological diagnoses that the patient brought, finding that she had been treated for a diagnosis that did not match with all her clinical sign and symptoms and this helped us to find the real cause(AU)

[Headache triggered exclusively by laughing, as a presenting symptom of a posterior fossa meningioma]. / Cefalea desencadenada exclusivamente por la risa, como forma de presentacion de un meningioma de fosa posterior.

TITLE: Cefalea desencadenada exclusivamente por la risa, como forma de presentacion de un meningioma de fosa posterior.

Cirugía neurológica en meningioma del tercio medio del ala del esfenoides. Presentación de un caso / Neurological surgery in meningioma of the middle third of the wing of the sphenoid. Presentation of a case

RESUMEN Se presentó un caso de una paciente de 70 años de edad, con antecedentes patológicos personales de hipertensión arterial controlada, además de un síndrome demencial instaurado hace 5 años aproximadamente. Con un diagnóstico presuntivo de una demencia tipo Alzheimer y sin estudios desde el punto de vista imagenológico. Se le realizaron diversos estudios que arrojaron una lesión extraaxial interpretada como un meningioma del tercio medio del ala del esfenoides. Se le aplicó una resección tumoral de la totalidad de la lesión, su evolución postquirúrgica fue satisfactoria.

ABSTRACT The case presented is the one of a female patient aged 70 years, with personal pathological antecedents of controlled arterial hypertension besides dementia syndrome for around five years, presumptively diagnosed as Alzheimer-kind dementia without imaging studies. She underwent several studies showing an extra axial lesion that was interpreted as meningioma of the medial third of the sphenoid wing. The tumor resection of the entire lesion was carried out; the post-surgery evaluation was satisfactory.

Graduação histológica e aspectos clínico-patológicos relacionados em 22 meningiomas de cães / Histological grading and related clinical and pathological aspects of 22 canine meningioma

Vinte e dois casos de meningiomas em cães, diagnosticados num período de aproximadamente 18 anos, foram revisados. Os neoplasmas foram graduados e classificados histologicamente de acordo com os critérios da Organização Mundial da Saúde (OMS de 2007) para meningiomas em humanos adaptados para cães, em Grau I (G-I; benignos), Grau II (G-II; atípicos) e Grau III (G-III; anaplásico ou maligno). Dos protocolos de necropsias foram retiradas adicionalmente informações referentes ao sexo, idade, raça, evolução clínica, sinais clínicos, localização anatômica e achados macroscópicos. Os meningiomas intracranianos supratentoriais foram os mais frequentes em relação às demais localizações intracranianas ou intraespinhais. Os intracranianos caracterizaram-se principalmente por sinais clínicos de alteração tálamo-cortical. Os intraespinhais caracterizaram-se principalmente por causarem ataxia. Meningiomas G-I foram os mais frequentes (63,6%) nos 22 cães, seguidos pelos G-III (22,7%) e G-II (13,6%). Os G-I caracterizaram-se por ter o subtipo psammomatoso como o mais frequente, mais de um padrão morfológico em um mesmo tumor, e um terço deles apresentando áreas de invasão do tecido nervoso, 71,4% dos casos acometendo fêmeas, uma média de idade de 11 anos, cães com raça definida como os mais acometidos e por ter o maior tempo de sobrevivência após a manifestação dos sinais clínicos. Os meningiomas G-II caracterizaram-se por ter o subtipo cordoide como o mais frequente, invasão do tecido nervoso em um terço dos casos, somente fêmeas acometidas, uma média de idade de 12 anos, dois terços dos cães acometidos sem raça definida e o tempo máximo de sobrevivência de 20 dias. Os meningiomas G-III caracterizaram-se por ter o subtipo papilar como o mais frequente, invasão do tecido nervoso em 80% dos casos, 60% dos casos acometendo fêmeas, uma média de idade de 8 anos, 80% dos cães acometidos da raça Boxer e o tempo máximo de sobrevivência de 90 dias...(AU)

Twenty two cases of meningiomas in dogs, diagnosed in about 18 years, were analyzed. The neoplasms were histologicaly classified and graded according to the World and Health Organization (WHO of 2007) for human meningiomas, adapted for dogs, in Grade I (G-I; benign), Grade II (G-II; atypical), and Grade III (G-III; anaplastic or malignant). Additional data about gender, age, breed, skull conformation, clinical course and signs, anatomic localization, gross and histological findings were obtained from the necropsy reports. Intracranial and supratentorial meningiomas were the most frequent in relation to the other intracranial or intraspinal sites. The intracranial ones were characterized mainly by clinical signs of thalamic-cortical alteration. Intraspinal ones were mainly characterized by ataxia. G-I meningiomas were the most frequent (63.6%) in dogs, followed by G-III (22.7%) and G-II (13.6%). GI were characterized by having the psammomatous subtype as the most frequent, more than one morphological pattern in the same tumor, one third presenting areas of invasion of nervous tissue, 71.4% of cases involving females, a mean age of 11 years, pure breed dogs as the most affected ones and for having the longest survival time after the manifestation of clinical signs. G-II meningiomas were characterized by having the chordoid subtype as the most frequent, invasion of nervous tissue in one third of cases, only females affected, a mean age of 12 years, two-thirds of the dogs affected were mongrels and the maximum survival time of 20 days. The G-III meningiomas were characterized by having the papillary subtype as the most frequent, invasion of the nervous tissue in 80% of the cases, 60% of the cases involving females, a mean age of 8 years, 80% of dogs affected were Boxers and the maximum survival time of 90 days. In conclusion, this study allowed to establish a relationship between the three histological grades observed in 22 cases of meningiomas in dogs...(AU)

Graduação histológica e aspectos clínico-patológicos relacionados em 22 meningiomas de cães / Histological grading and related clinical and pathological aspects of 22 canine meningioma

Vinte e dois casos de meningiomas em cães, diagnosticados num período de aproximadamente 18 anos, foram revisados. Os neoplasmas foram graduados e classificados histologicamente de acordo com os critérios da Organização Mundial da Saúde (OMS de 2007) para meningiomas em humanos adaptados para cães, em Grau I (G-I; benignos), Grau II (G-II; atípicos) e Grau III (G-III; anaplásico ou maligno). Dos protocolos de necropsias foram retiradas adicionalmente informações referentes ao sexo, idade, raça, evolução clínica, sinais clínicos, localização anatômica e achados macroscópicos. Os meningiomas intracranianos supratentoriais foram os mais frequentes em relação às demais localizações intracranianas ou intraespinhais. Os intracranianos caracterizaram-se principalmente por sinais clínicos de alteração tálamo-cortical. Os intraespinhais caracterizaram-se principalmente por causarem ataxia. Meningiomas G-I foram os mais frequentes (63,6%) nos 22 cães, seguidos pelos G-III (22,7%) e G-II (13,6%). Os G-I caracterizaram-se por ter o subtipo psammomatoso como o mais frequente, mais de um padrão morfológico em um mesmo tumor, e um terço deles apresentando áreas de invasão do tecido nervoso, 71,4% dos casos acometendo fêmeas, uma média de idade de 11 anos, cães com raça definida como os mais acometidos e por ter o maior tempo de sobrevivência após a manifestação dos sinais clínicos. Os meningiomas G-II caracterizaram-se por ter o subtipo cordoide como o mais frequente, invasão do tecido nervoso em um terço dos casos, somente fêmeas acometidas, uma média de idade de 12 anos, dois terços dos cães acometidos sem raça definida e o tempo máximo de sobrevivência de 20 dias. Os meningiomas G-III caracterizaram-se por ter o subtipo papilar como o mais frequente, invasão do tecido nervoso em 80% dos casos, 60% dos casos acometendo fêmeas, uma média de idade de 8 anos, 80% dos cães acometidos da raça Boxer e o tempo máximo de sobrevivência de 90 dias. Este estudo permitiu estabelecer uma relação entre os três graus histológicos observados em 22 casos de meningiomas em cães com vários parâmetros clínico-epidemiológicos e patológicos, fornecendo informações úteis para um melhor conhecimento da correlação entre a graduação histológica e a evolução clínica desses neoplasmas.(AU)

Twenty two cases of meningiomas in dogs, diagnosed in about 18 years, were analyzed. The neoplasms were histologicaly classified and graded according to the World and Health Organization (WHO of 2007) for human meningiomas, adapted for dogs, in Grade I (G-I; benign), Grade II (G-II; atypical), and Grade III (G-III; anaplastic or malignant). Additional data about gender, age, breed, skull conformation, clinical course and signs, anatomic localization, gross and histological findings were obtained from the necropsy reports. Intracranial and supratentorial meningiomas were the most frequent in relation to the other intracranial or intraspinal sites. The intracranial ones were characterized mainly by clinical signs of thalamic-cortical alteration. Intraspinal ones were mainly characterized by ataxia. G-I meningiomas were the most frequent (63.6%) in dogs, followed by G-III (22.7%) and G-II (13.6%). GI were characterized by having the psammomatous subtype as the most frequent, more than one morphological pattern in the same tumor, one third presenting areas of invasion of nervous tissue, 71.4% of cases involving females, a mean age of 11 years, pure breed dogs as the most affected ones and for having the longest survival time after the manifestation of clinical signs. G-II meningiomas were characterized by having the chordoid subtype as the most frequent, invasion of nervous tissue in one third of cases, only females affected, a mean age of 12 years, two-thirds of the dogs affected were mongrels and the maximum survival time of 20 days. The G-III meningiomas were characterized by having the papillary subtype as the most frequent, invasion of the nervous tissue in 80% of the cases, 60% of the cases involving females, a mean age of 8 years, 80% of dogs affected were Boxers and the maximum survival time of 90 days. In conclusion, this study allowed to establish a relationship between the three histological grades observed in 22 cases of meningiomas in dogs with various clinical-epidemiological and pathological parameters, providing useful information for a better understanding of the correlation between the histological grading and the clinical evolution of these neoplasms.(AU)

Necrosis is a consistent factor to recurrence of meningiomas: should it be a stand-alone grading criterion for grade II meningioma?

The purpose of this study was to evaluate spontaneous necrosis as a possible isolated factor for progression and recurrence in grade I meningiomas classified according to the current World Health Organization (WHO) classification. Meningiomas are the most frequently reported primary intracranial tumours, accounting for more than 35%. The 2016 WHO classification of central nervous system tumors stratifies meningiomas in grades I (benign), II (atypical), and III (malignant), according to histopathological aspects and the risk of progression or recurrence. Among 110 patients with intracranial meningiomas, 70 were WHO grade I meningiomas with no findings of atypia (G1WON), 15 were WHO grade I with necrosis (G1WN), 21 were WHO grade II (G2), and 4 were WHO grade III (G3). The mean follow-up was 5.9 ± 0.2 years. High performance scale (KPS ≥ 80) was different (p < 0.001) between WHO grade I meningiomas without (81.4%) and with (60%) necrosis. The 5-year mortality rate was 1.4, 6.7 and 5.9% for G1WON, G1WN and G2, respectively, with significant difference (p = 0.011) related to the presence of necrosis. The risk of recurrence was 3.7 times higher in G1WN than in G1WON (p = 0.017), and 4.2 times in G2 (p = 0.010). Progression-free survival (PFS) was clearly higher in patients with G1WON compared to G1WN and G2 (p = 0.002 and p < 0.001, respectively). There was no significant difference in PFS between G1WN and G2 (p = 0.692). Retreatment was also superior in meningioma with necrosis. Our findings provide clear statistical data to consider that patients with benign meningiomas and histologic findings of spontaneous necrosis are at increased risk of progression and recurrence compared to those with benign lesion without atypical features. Statistical analysis curves also suggest that these lesions behave more similarly to those currently classified as WHO grade II meningioma.

Surgical Treatment of Rosai-Dorfman Intracranial Disease: Case Report and Literature Review

Rosai-Dorfman disease is a benign lymphoproliferative disease with rare occurrence in the overall population. The characteristic findings of the disease are emperipolesis on microscopy and S-100 protein positivity on immunohistochemistry. The present report describes the case of a 57-year-old man who presented with repeated seizures, urinary retention, and ataxia. Satisfactory results were obtained with surgical treatment. The diagnosis was confirmed by immunohistochemistry.