autoimmune hypophysitis/horúčka

Odkaz sa uloží do schránky

ČlánkyKlinické štúdiePatenty

Vyberte typ zoradenia

15 výsledky

[A clinically diagnosed lymphocytic hypophysitis presenting as recurrent meningitis].

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

A 55-year-old woman was admitted to our hospital complaining of severe headache with fever and apparent neck stiffness. Neutrophilic pleocytosis was demonstrated in cerebrospinal fluid (CSF) and bacterial meningitis was strongly suspected, but bacterial culture of CSF was negative. After the

A relapsing remitting lymphocytic hypophysitis.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

Lymphocytic Hypophysitis is a rare autoimmune disease of the pituitary presenting mainly with features of a mass lesion and loss of pituitary function. Its course is quite unpredictable and its treatment is still controversial as experience in the field remains scarce. We describe a 45 year-old

Lymphocytic hypophysitis with associated thyroiditis in a man with aseptic meningitis.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

OBJECTIVE Lymphocytic hypophysitis (LH) is a rare chronic inflammatory disorder characterized by lymphocytic infiltration of the pituitary gland commonly affecting women during pregnancy or post-partum period. The pathogenesis remains uncertain, however an autoimmune process is frequently

Idiopathic granulomatous hypophysitis: a systematic review of 82 cases in the literature.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

Idiopathic granulomatous hypophysitis (IGH) is a rare inflammatory disease of the pituitary. There is debate in the scientific literature as to whether IGH represents a continuum of disease with lymphocytic hypophysitis or has a distinct pathogenesis. Due to the rare nature of the disease, previous

Giant cell myocarditis with central diabetes insipidus: A case report.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

A 51-year-old male, previously diagnosed with central diabetes insipidus due to lymphocytic hypophysitis, presented with fever and dyspnea for 1 week. On arrival, he exhibited hypotension (85/60 mmHg) and sinus tachycardia (110 bpm). His electrocardiogram revealed mild ST elevation on V2-V4.

Inflammatory hypophysitis - the spectrum of disease.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

BACKGROUND Inflammatory conditions of the pituitary are rare and consequently there are a number of single case reports of this condition but few reports of series. The condition is often divided into lymphocytic and granulomatous hypophysitis and it has been suggested that these two conditions

Hypopituitarism associated with transient diabetes insipidus followed by an episode of painless thyroiditis in a young man.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

A 16-year-old male complained of a headache and a high fever followed by polyuria. The endocrinological studies showed he had hypopituitarism and central diabetes insipidus, and magnetic resonance imaging (MRI) revealed a pituitary mass. Diabetes insipidus gradually improved and hydrocortisone

Petrified auricular cartilages pointing the diagnosis of post-partum hypopituitarism in an encephalopathic patient.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

True ossification of ear auricles is exceptional. We present the first case linking this finding to post-partum hypopituitarism. A 57-year-old female presented with a 2-day history of fever, headache and behavioural disturbances. Brain magnetic resonance imaging was normal. Since cerebral spinal

Elevated bone resorption markers in a patient with hypercalcemia associated with post-partum thyrotoxicosis and hypoadrenocorticism due to pituitary failure.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

A 36-yr-old woman began to suffer from headache, anorexia and general fatigue at 35 weeks' gestation. About 2 or 3 months after the delivery, fever, tachycardia and generalized musculoskeletal disorder appeared. Thereafter, they worsened rapidly, accompanied by a disturbance of consciousness and

[Malignant lymphoma with IgG4-related disease arising in a very elderly man]

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

IgG4-related disease (IgG4-RD) which is characterized by an autoimmune abnormality and elevated serum IgG4 level often presents as swelling, nodules, and the thickening of multiple organs. It typically occurs in middle-aged to elderly patients, but its pathogenesis remains unclear. Lymphadenopathy

[Spontaneous remission of acromegaly after meningitis: a case report].

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

There have been several reports describing the cases of acromegaly, which show reduction in size of tumor in due to pituitary apoplexy or lymphocytic hypophysitis. We have encountered a patient of acromegaly, who developed panhypopituitarism after suffering from meningitis and showed the reduction

[Lymphocytic infundibulo-hypophysitis with diabetes insipidus as a new clinical entity: a case report and review of the literature].

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

In 1992, we reported a lymphocytic adenohypophysitis (LIH) (Neurol Med Chir). We considered this case unusual in that the case was that of a menopausal female and that it was accompanied with diabetes insipidus as classical lymphocytic adenohypohysitis (LAH). Subsequently, Ahmed reported two cases

A rare cause of postpartum acute hyponatremia.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

A previously healthy 24-year-old female underwent an emergent caesarean section without a major bleeding described. During the first post-operative days (POD) she complained of fatigue, headache and a failure to lactate with no specific and conclusive findings on head CT. On the following days,

Autoimmune polyendocrinopathy and hypophysitis after Puumala hantavirus infection.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

Puumala hantavirus (PUUV) infection causes nephropathia epidemica (NE), a relatively mild form of haemorrhagic fever with renal syndrome (HFRS). Hypophyseal haemorrhage and hypopituitarism have been described in case reports on patients with acute NE. Chronic hypopituitarism diagnosed months or

Diagnosis and management of tumor-like hypophysitis: A retrospective case series.

Články môžu prekladať iba registrovaní používatelia

Prihlásiť Registrácia

Tumor-like hypophysitis is an uncommon sellar condition that presents as inflammatory lesions on the structures of the pituitary gland. The diagnosis and management of hypophysitis poses a significant challenge, as its clinical manifestation and appearance in imaging studies are difficult to

Pripojte sa k našej
facebookovej stránke

Herbal & Natural Medicine

Najkompletnejšia databáza liečivých bylín podporovaná vedou

Pracuje v 55 jazykoch
Bylinné lieky podporené vedou
Rozpoznávanie bylín podľa obrázka
Interaktívna GPS mapa - označte byliny na mieste (už čoskoro)
Prečítajte si vedecké publikácie týkajúce sa vášho hľadania
Vyhľadajte liečivé byliny podľa ich účinkov
Usporiadajte svoje záujmy a držte krok s novinkami, klinickými skúškami a patentmi

Zadajte príznak alebo chorobu a prečítajte si o bylinách, ktoré by vám mohli pomôcť, napíšte bylinu a pozrite sa na choroby a príznaky, proti ktorým sa používa.
* Všetky informácie sú založené na publikovanom vedeckom výskume