Cushing
Mostrando 1-12 de 256 artigos, teses e dissertações.
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1. Qual a abordagem inicial para avaliação de oligomenorréia após a menarca?
Na puberdade, o sangramento uterino anormal é geralmente disfuncional (endócrino). Deve-se realizar uma anamnese minuciosa do histórico menstrual da adolescente. Se a menarca ocorreu na idade esperada, e se desde então os ciclos têm se apresentado irregulares no que diz respeito ao período e duração (como por exemplo oligomenorréia, ou seja, cicl
Núcleo de Telessaúde Rio Grande do Sul. Publicado em: 12/06/2023
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2. Quais são as indicações de encaminhamento para cirurgia bariátrica?
O tratamento cirúrgico da obesidade (cirurgia bariátrica) pode ser indicado nos pacientes com IMC ≥ 40kg/m² ou em pacientes com IMC ≥ 35 associado a comorbidades como: risco cardiovascular maior que 20% em dez anos, doença cardiovascular, hipertensão arterial de difícil controle, diabetes mellitus de difícil controle, síndrome da apneia e hipo
Núcleo de Telessaúde Rio Grande do Sul. Publicado em: 12/06/2023
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3. Quais os valores de referência para glicosúria?
No exame quantitativo de urina coletada ao acaso, o valor de referência da glicose é menor que 30mg/dl
. Habitualmente é indetectável
. A glicosúria só ocorre quando os níveis de glicemia atingem 180 a 200mg/dl. Geralmente, decorre do diabetes mellitus, mas pode ocorrer em outras situações, como dietas ricas em glicose antes da coleta
Núcleo de Telessaúde Bahia. Publicado em: 12/06/2023
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4. Como deve ser o manejo do corticóide em casos de Febre Chikungunya?
Os corticosteroides são contraindicados na fase aguda da febre Chikungunya .
Nas fases subaguda e crônica, o uso de corticóides está indicado apenas para os casos com dor articular não responsiva a AINE (Anti-Inflamatórios Não Esteroidais) e analgésicos, em pacientes com dor moderada a intensa, poliarticular e debilitante.
Para os caso
Núcleo de Telessaúde NUTES PE. Publicado em: 12/06/2023
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5. Quais são as causas e quando devemos tratar a hipertrigliceridemia?
Casos leves (entre 150 e 199 mg/dL) a moderados (entre 200 e 999 m/dL) estão relacionados à dislipidemia poligênica e a hábitos de vida. Casos graves (entre 1000 e 1999 mg/dL) e muito graves (acima de 2000 mg/dL) podem dever-se a causa secundária ou dislipidemia primária de padrão familiar.
As principais causas a serem consideradas são: hipe
Núcleo de Telessaúde Rio Grande do Sul. Publicado em: 12/06/2023
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6. A case of subcutaneous sarcoidosis in a patient with Cushing’s syndrome
Abstract A 41-year-old female visited our department complaining of asymptomatic subcutaneous nodules on the right forearm. She had been diagnosed as having Cushing syndrome due to an adrenal tumor 5-months previously. After she underwent surgery for the adrenal tumor, the subcutaneous nodules gradually increased in number. Physical examination showed ill-de
Anais Brasileiros de Dermatologia. Publicado em: 2022
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7. Cushing’s syndrome due to ectopic adrenocorticotropin secretion by a parotid carcinoma
SUMMARY We report a rare case of Cushing’s syndrome in a 37-year-old female who initially presented with localized acinic cell carcinoma of the parotid gland. In January 2014, she underwent a right parotidectomy with facial nerve preservation and adjuvant radiotherapy. In August 2018, she presented a histologically-proven local regional relapse. The patien
Archives of Endocrinology and Metabolism. Publicado em: 2022
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8. Cushing disease due to a somatic USP8 mutation in a patient with evolving pituitary hormone deficiencies due to a germline GH1 splicing variant
SUMMARY We present the unique case of an adult Brazilian woman with severe short stature due to growth hormone deficiency with a heterozygous G to T substitution in the donor splice site of intron 3 of the growth hormone 1 (GH1) gene (c.291+1G>T). In this autosomal dominant form of growth hormone deficiency (type II), exon 3 skipping results in expression of
Archives of Endocrinology and Metabolism. Publicado em: 2022
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9. A novel mutation in PRKAR1A gene in a patient with Carney complex presenting with pituitary macroadenoma, acromegaly, Cushing's syndrome and recurrent atrial myxoma
SUMMARY Carney complex (CNC) is a rare syndrome of multiple endocrine and non-endocrine tumors. In this paper we present a 23-year-old Iranian woman with CNC who harbored a novel mutation (c.642dupT) in PRKAR1A gene. This patient presented with pituitary macroadenoma, acromegaly, recurrent atrial myxoma, Cushing's syndrome secondary to primary pigmented nodu
Arch. Endocrinol. Metab.. Publicado em: 2021-06
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10. Ectopic Cushing syndrome in Colombia
ABSTRACT Objective The aim was to describe the clinical features of patients with ectopic Cushing syndrome (ECS) from Colombia and compare these findings with other series to provide the best management for these patients. Materials and methods Records of patients with ECS from 1986 to 2017 were retrospectively reviewed; patients with a diagnosis of adre
Arch. Endocrinol. Metab.. Publicado em: 2020-12
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11. Personalized approach to growth hormone replacement in adults
ABSTRACT Growth hormone (GH) deficiency (GHD) in adults is well-characterized and includes abnormal body composition, reduced bone mass, an adverse cardiovascular risk profile, and impaired quality of life. In the early 1990s, it was also shown that patients with hypopituitarism without GH replacement therapy (GHRT) had excess mortality. Today, GHRT has been
Arch. Endocrinol. Metab.. Publicado em: 10/01/2020
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12. Long-term outcome after bilateral adrenalectomy in Cushing’s disease with focus on Nelson’s syndrome
ABSTRACT Objective We analyzed the clinical, biochemical, and imaging findings of adrenalectomized patients with Cushing’s disease (CD) in order to compare the characteristics of those who developed Nelson’s syndrome (NS) versus those who did not develop this complication (NNS), aiming to identify possible predictive factors for its occurrence. Subjec
Arch. Endocrinol. Metab.. Publicado em: 27/06/2019