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Patricia Fainstein Day
Hospital Italiano de Buenos Aires
EndocrinologyPathologyAcromegalyDiabetes mellitusMedicine
22Publications
8H-index
190Citations
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Publications 20
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#1Karina DanilowiczH-Index: 11
#2Soledad SosaH-Index: 1
Last. Fabián PitoiaH-Index: 14
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#1María Belén Bosco Schamun (Hospital Italiano de Buenos Aires)H-Index: 1
#2Ricardo CorreaH-Index: 1
Last. Patricia Fainstein DayH-Index: 8
view all 5 authors...
Abstract Carney complex is a multiple neoplasia syndrome having endocrine and non-endocrine manifestations. Diagnostic criteria include myxoma, lentigines, and primary pigmented nodular adrenocortical disease, amongst other signs/symptoms. In most cases it is an autosomal dominant disease, and diagnosis therefore requires study and follow-up of the family members. Inactivating mutations of the PRKAR1A gene were identified as the main cause of the disease, although since 2015 other disease-relate...
1 CitationsSource
#1María Belén Bosco Schamun (Hospital Italiano de Buenos Aires)H-Index: 1
#2Ricardo CorreaH-Index: 1
Last. Patricia Fainstein DayH-Index: 8
view all 5 authors...
El complejo de Carney es un sindrome de neoplasia multiple de tumores endocrinos y no endocrinos, que incluye la presencia de mixoma, lentiginosis cutanea y enfermedad nodular primaria pigmentada, entre otros criterios para el diagnostico.
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Resumen Introduccion El riesgo de desarrollar neoplasias colonicas en pacientes acromegalicos y su relacion directa con los niveles elevados de GH/IGF-1 no estan bien establecidos y continuan siendo motivo de controversia en la literatura mundial. El objetivo de este trabajo fue evaluar el riesgo de desarrollar lesiones neoplasicas avanzadas (LNA) (adenomas mayores a 1 cm, componente velloso mayor del 75% y/o displasia de alto grado), en pacientes con acromegalia, comparado con un grupo control....
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#1Patricia Fainstein Day (Hospital Italiano de Buenos Aires)H-Index: 8
#2Monica Graciela Loto (Hospital Italiano de Buenos Aires)H-Index: 5
Last. Diego Giunta (Hospital Italiano de Buenos Aires)H-Index: 11
view all 6 authors...
Objectives The main purpose of this study was to estimate the incidence rate and prevalence of clinically relevant pituitary adenomas (PAs) within the Hospital Italiano Medical Care Program (HIMCP), a well-defined population of 150,000 members living in the urban and suburban area of the city of Buenos Aires. We defined clinically relevant PAs as those associated with endocrine dysfunction and/or mass effect. Subjects and methods A retrospective open cohort study was conducted, including all mem...
15 CitationsSource
#1Karina Danilowicz (UBA: University of Buenos Aires)H-Index: 11
Last. Oscar D. Bruno (UBA: University of Buenos Aires)H-Index: 16
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Introduction Acromegaly is a rare disease with a large burden due its associated comorbidities and the life-long management required. Since the occurrence and severity of associated complications are related to length of exposure to the excess growth hormone seen in acromegaly, early diagnosis is imperative. The delay in diagnosis, however, can be long, and may be the result of a lack of disease awareness and screening programs. Since acromegaly is an uncommon disease, finding ways to increase r...
1 CitationsSource
Objetive The aim was to assess the evolution of tumor size and prolactin (PRL) levels in patients with micro and macroprolactinomas diagnosed and treated with dopamine agonists during fertile age, and the effects of suspension of drugs after menopause. Retrospective study, 29 patients with prolactinomas, 22 microadenomas and 7 macroadenomas, diagnosed during their fertile age were studied in their menopause; treatment was stopped in this period. Age at menopause was 49 ± 3.6 years. The average t...
4 CitationsSource
#1Maria Lorena VialeH-Index: 1
Last. Oscar BrunettoH-Index: 1
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IgG4-related hypophysitis is a recently described entity belonging to the group of IgG4-related diseases. Many other organs can also be affected, and it is more common in older men. To date, 32 cases of IgG4-related hypophysitis have been reported in the literature, 11 of which included confirmatory tissue biopsy and the majority affecting multiple organs. The aim of this report is to present two cases of biopsy-proven IgG4-related hypophysitis occurring in two young female patients with no evid...
14 CitationsSource
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