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1.
Life (Basel) ; 13(1)2023 Jan 05.
Article in English | MEDLINE | ID: mdl-36676107

ABSTRACT

There is evidence of association between sellar barrier thickness and intraoperative cerebrospinal fluid (CSF) leakage, impacting the postoperative prognosis of the patients. The aim of this study is to analyze the clinical applicability of the sellar barrier concept in a series of operated patients with pituitary apoplexy (PA). A retrospective study was conducted including 47 patients diagnosed with PA who underwent surgical treatment through a transsphenoidal approach. Brain magnetic resonance imaging (MRI) of the patients were evaluated and classified utilizing the following criteria: strong barrier (greater than 1 mm), weak barrier (less than 1 mm), and mixed barrier (less than 1 mm in one area and greater than 1 mm in another). The association between sellar barrier types and CSF leakage was analyzed, both pre- and intraoperatively. The preoperative MRI classification identified 10 (21.28%) patients presenting a weak sellar barrier, 20 patients (42.55%) with a mixed sellar barrier, and 17 patients (36.17%) exhibiting a strong sellar barrier. Preoperative weak and strong sellar barrier subtypes were associated with weak (p ≤ 0.001) and strong (p = 0.009) intraoperative sellar barriers, respectively. Strong intraoperative sellar barrier subtypes reduced the odds of CSF leakage by 86% (p = 0.01). A correlation between preoperative imaging and intraoperative findings in the setting of pituitary apoplexy has been observed.

2.
Neurocirugía (Soc. Luso-Esp. Neurocir.) ; 32(2): 62-68, mar.- apr. 2021. ilus, tab, graf
Article in Spanish | IBECS | ID: ibc-222443

ABSTRACT

Objetivo Los hemangiopericitomas intracraneanos (HPC) son tumores de muy baja frecuencia, alta recidiva local y riesgo de metástasis extracraneal. El objetivo del siguiente trabajo es presentar los resultados en el tratamiento de los HPC en nuestra institución en los últimos 20 años y realizar una revisión de la literatura del tema. Material y métodos Se realizó un estudio retrospectivo que incluyó a los pacientes con diagnóstico de tumor fibroso solitario/hemangiopericitoma (TFS/HPC) intracraneanos intervenidos quirúrgicamente en el periodo 1997-2017. Se incluyeron pacientes con inmunomarcación positiva para STAT-6 y grado histológico II-III. Se recabaron datos demográficos, características tumorales, tratamiento y sobrevida de estos pacientes. Resultados Un total de 19 pacientes cumplieron los criterios de inclusión. La mediana de seguimiento fue de 96 meses (12-230). La mortalidad fue del 21% (n = 4). El 57,9% presentaron al menos una recidiva tumoral (n = 11) (con una recurrencia del 6, del 67 y del 90% a 1, 5 y 10 años, respectivamente). Cinco pacientes presentaron metástasis extracraneal. Tuvieron mayor sobrevida los pacientes con tumores < 6 cm (p < 0,05). Conclusiones Se presentó una serie de pacientes operados de TFS/HPC según los nuevos criterios de la OMS. El tamaño es un factor predictor de sobrevida. Actualmente no existen criterios validados de resección quirúrgica en esta patología. Una clasificación con orientación quirúrgica sería de utilidad en el futuro (AU)


Objective Intracranial hemangiopericytoma (HPC) is a rare central nervous system tumor characterized by its low incidence, high rate of local recurrence and risk of metastasis. The main objectives of this paper are two: to show the results in the treatment of HPC in our institution in the last 20 years and to make a review of the literature on this topic. Methods Retrospective review that includes patients diagnosed with intracranial solitary fibrous tumor/hemangiopericytoma (SFT/HPC) that have undergone surgery from 1997 to 2017. It includes patients that had nuclear expression of STAT-6 (detected by immunohistochemistry) and grade II/III histopathological diagnosis (defined by the World Health Organization in 2016). We collected demographic data, tumor characteristics, treatment and survival of these patients. Results A total of 19 patients fulfilled inclusion criteria. The median follow up was 96 months (12-230). The mortality rate was 21% (n = 4). 57.9% of patients presented at least one tumor recurrence (n = 11) (recurrences of 6%, 67% y 90% at 1, 5 and 10 years). Five patients presented extracranial metastasis. Patients with tumors < 6 cm had greater survival (P < .05). Conclusions A series of patients undergoing SFT/HPC were presented according to the new WHO criteria. Size is a predictor of survival. Currently there are no validated criteria for surgical resection in this pathology. A classification with surgical guidance would be useful (AU)


Subject(s)
Humans , Male , Female , Adolescent , Young Adult , Adult , Middle Aged , Hemangiopericytoma/surgery , Brain Neoplasms/surgery , Retrospective Studies , Treatment Outcome , Kaplan-Meier Estimate , Prognosis
3.
Neurocirugia (Astur : Engl Ed) ; 32(2): 62-68, 2021.
Article in English, Spanish | MEDLINE | ID: mdl-32473774

ABSTRACT

OBJECTIVE: Intracranial hemangiopericytoma (HPC) is a rare central nervous system tumor characterized by its low incidence, high rate of local recurrence and risk of metastasis. The main objectives of this paper are two: to show the results in the treatment of HPC in our institution in the last 20years and to make a review of the literature on this topic. METHODS: Retrospective review that includes patients diagnosed with intracranial solitary fibrous tumor/hemangiopericytoma (SFT/HPC) that have undergone surgery from 1997 to 2017. It includes patients that had nuclear expression of STAT-6 (detected by immunohistochemistry) and gradeII/III histopathological diagnosis (defined by the World Health Organization in 2016). We collected demographic data, tumor characteristics, treatment and survival of these patients. RESULTS: A total of 19 patients fulfilled inclusion criteria. The median follow up was 96 months (12-230). The mortality rate was 21% (n=4). 57.9% of patients presented at least one tumor recurrence (n=11) (recurrences of 6%, 67% y 90% at 1, 5 and 10years). Five patients presented extracranial metastasis. Patients with tumors <6cm had greater survival (P<.05). CONCLUSIONS: A series of patients undergoing SFT/HPC were presented according to the new WHO criteria. Size is a predictor of survival. Currently there are no validated criteria for surgical resection in this pathology. A classification with surgical guidance would be useful.


Subject(s)
Hemangiopericytoma , Solitary Fibrous Tumors , Hemangiopericytoma/surgery , Humans , Neoplasm Recurrence, Local , Prognosis , Retrospective Studies , Solitary Fibrous Tumors/surgery
4.
Arq Neuropsiquiatr ; 76(3): 139-144, 2018 Mar.
Article in English | MEDLINE | ID: mdl-29809232

ABSTRACT

Background Primary central nervous system lymphomas (PCNSL) are infrequent. The traditional treatment of choice is chemotherapy. Complete resections have generally not been recommended, because of the risk of permanent central nervous system deficits with no proven improvement in survival. The aim of the current study was to compare survival among patients with PCNSL who underwent biopsy versus surgical resection. Methods A retrospective study was conducted on 50 patients with a confirmed diagnosis of PCNSL treated at our center from January 1994 to July 2015. Results Patients in the resection group exhibited significantly longer median survival time, relative to the biopsy group, surviving a median 31 months versus 14.5 months; p = 0.016. Conclusions In our series, patients who had surgical resection of their tumor survived a median 16.5 months longer than patients who underwent biopsy alone.


Subject(s)
Central Nervous System Neoplasms/surgery , Lymphoma/surgery , Adult , Aged , Aged, 80 and over , Biopsy , Central Nervous System Neoplasms/immunology , Central Nervous System Neoplasms/mortality , Central Nervous System Neoplasms/pathology , Female , Humans , Immunocompetence , Kaplan-Meier Estimate , Lymphoma/immunology , Lymphoma/mortality , Lymphoma/pathology , Male , Middle Aged , Retrospective Studies , Risk Factors , Time Factors , Treatment Outcome
5.
Arq. neuropsiquiatr ; 76(3): 139-144, Mar. 2018. tab, graf
Article in English | LILACS | ID: biblio-888366

ABSTRACT

ABSTRACT Background Primary central nervous system lymphomas (PCNSL) are infrequent. The traditional treatment of choice is chemotherapy. Complete resections have generally not been recommended, because of the risk of permanent central nervous system deficits with no proven improvement in survival. The aim of the current study was to compare survival among patients with PCNSL who underwent biopsy versus surgical resection. Methods A retrospective study was conducted on 50 patients with a confirmed diagnosis of PCNSL treated at our center from January 1994 to July 2015. Results Patients in the resection group exhibited significantly longer median survival time, relative to the biopsy group, surviving a median 31 months versus 14.5 months; p = 0.016. Conclusions In our series, patients who had surgical resection of their tumor survived a median 16.5 months longer than patients who underwent biopsy alone.


RESUMO Introducción Los linfomas primarios del sistema nervioso central (LPSNC) son infrecuentes. Tradicionalmente el tratamiento de elección es la quimioterapia. Existe un paradigma de no indicar resección, por el riesgo de déficit neurológico sin aumento de la sobrevida. El objetivo del presente estudio es comparar la sobrevida de pacientes con LPSNC sometidos a biopsia versus resección. Métodos Estudio retrospectivo que incluye 50 pacientes con diagnóstico confirmado de LPSNC tratados en nuestra Institución desde enero de 1994 hasta julio de 2015. Resultados Los pacientes del "grupo resección" mostraron una sobrevida media significativamente mayor respecto a los del "grupo biopsia"; 31 meses versus 14,5 meses respectivamente, p = 0,016. Conclusiones En nuestra serie, los pacientes que con resección quirúrgica de su tumor tuvieron una sobrevida media de 16,5 meses superior que los pacientes biopsiados.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged , Aged, 80 and over , Central Nervous System Neoplasms/surgery , Lymphoma/surgery , Time Factors , Biopsy , Retrospective Studies , Risk Factors , Treatment Outcome , Central Nervous System Neoplasms/immunology , Central Nervous System Neoplasms/mortality , Central Nervous System Neoplasms/pathology , Kaplan-Meier Estimate , Immunocompetence , Lymphoma/immunology , Lymphoma/mortality , Lymphoma/pathology
8.
Rev. argent. dermatol ; 66(1): 1-7, ene.-mar. 1985. ilus, Tab
Article in Spanish | BINACIS | ID: bin-36874

ABSTRACT

Se refieren 95 casos de leishmaniasis infantil, estudiados en los Servicios de las Cátedras de Enfermedades Infecciosas y Dermatología de la Universidad Nacional de Tucumán. La edad de los enfermos oscilaba entre algunos meses y 15 años. El 52.63 por ciento pertenecen a la provincia de Tucumán, el 42.11 por ciento a la de Santiago del Estero y 5.26 por ciento a la de Salta. Merece ser destacado que en el 10.66 por ciento de nuestros enfermos se presentaban lesiones cutáneo-mucosas en labios, nariz y boca, muy destructivas, con caracteres similares a las que estamos acostumbrados a observar en la leishmaniasis del adulto (AU)


Subject(s)
Infant , Child, Preschool , Child , Adolescent , Humans , Male , Female , Leishmaniasis, Mucocutaneous/epidemiology , Leishmaniasis/epidemiology , Argentina
9.
Rev. argent. dermatol ; 66(1): 1-7, ene.-mar. 1985. ilus, tab
Article in Spanish | LILACS | ID: lil-2362

ABSTRACT

Se refieren 95 casos de leishmaniasis infantil, estudiados en los Servicios de las Cátedras de Enfermedades Infecciosas y Dermatología de la Universidad Nacional de Tucumán. La edad de los enfermos oscilaba entre algunos meses y 15 años. El 52.63 por ciento pertenecen a la provincia de Tucumán, el 42.11 por ciento a la de Santiago del Estero y 5.26 por ciento a la de Salta. Merece ser destacado que en el 10.66 por ciento de nuestros enfermos se presentaban lesiones cutáneo-mucosas en labios, nariz y boca, muy destructivas, con caracteres similares a las que estamos acostumbrados a observar en la leishmaniasis del adulto


Subject(s)
Infant , Child, Preschool , Child , Adolescent , Humans , Male , Female , Leishmaniasis/epidemiology , Leishmaniasis, Mucocutaneous/epidemiology , Argentina
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