hypophysitis/בחילה

הקישור נשמר בלוח

מאמריםניסויים קלינייםפטנטים

בחר סוג מיון

עמוד 1 מ 17 תוצאות

IgG4-related hypophysitis presenting as a pituitary adenoma with systemic disease.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Hypophysitis is a rare inflammatory disorder that can mimic a pituitary tumor clinically or radiologically. Furthermore, immunoglobulin G4 (IgG4)-related systemic disease is only a just recently characterized disorder. It can manifest as a systemic disease involving multiple organs, including the

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

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

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

Clinical course of a pituitary macroadenoma in the first trimester of pregnancy: probable lymphocytic hypophysitis.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Recent findings revealed that the clinical features of lymphocytic hypophysitis are more complicated than previously thought. It is rarely described in the first trimester of pregnancy and signs of meningeal irritation are infrequently reported. In this study, a pregnant woman in her first trimester

A case of hypopituitarism associated with Hashimoto's thyroiditis and candidiasis: lymphocytic hypophysitis or Sheehan's syndrome?

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Sheehan's syndrome and lymphocytic hypophysitis often occur in relation to pregnancy, making their differentiation difficult. We describe a 52-yr-old woman with hypopituitarism, Hashimoto's thyroiditis and candidiasis. She was admitted to our hospital because of nausea, vomiting and constipation.

Immunotherapy-induced autoimmune hypophysitis.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Autoimmune hypophysitis is an immune-related adverse event of immune checkpoint inhibitors. In this article, we present the case of a 58-year-old female patient who presented to the emergency room with gradually worsening nonspecific symptoms of headache, nausea, vomiting and decreased oral intake

Idiopathic giant-cell granulomatous hypophysitis mimicking acute meningitis.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

A 32-year-old woman presented with severe headache, photophobia, fever, nausea, vomiting, and worsening vision. She had also noted several months of amenorrhea. She was febrile to 38.9 degrees C. Laboratory evaluation revealed a markedly elevated erythrocyte sedimentation rate. Lumbar puncture

A Remarkable Response of Granulomatous Hypophysitis to Infliximab in a Patient With a Background of Crohn's Disease-A Case Report

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Background: Hypophysitis is primary or idiopathic or secondary to another disease process. The histologic subtypes of hypophysitis are lymphocytic, granulomatous, xanthomatous, xanthogranulomatous, or IgG4-related. Granulomatous hypophysitis is the second most common form and is characterized

Lymphocytic hypophysitis in a patient with systemic lupus erythematosus.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

A case of lymphocytic hypophysitis in a patient with systemic lupus erythematosus is described. A 20-year-old woman was admitted to our hospital with generalized myalgia and facial rash in May 1998. The patient had a medical history, physical examination, and laboratory findings compatible with

Granulomatous hypophysitis causing compression of the internal carotid arteries reversible with azathioprine and rituximab treatment.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Compression of the internal carotid artery (ICA) in the cavernous sinus area is a rare event and is mostly associated with pituitary adenomas and meningiomas. Other causes of ICA compression are less well known. We present a rare case of granulomatous hypophysitis causing compression

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

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

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

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

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

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

Xanthomatous hypophysitis.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Inflammatory lesions of the hypophysis include lymphocytic hypophysitis, pituitary abscess, and granulomatous inflammation, with or without specific infections (i.e., sarcoidosis, mycobacteria). These lesions are known to mimic pituitary neoplasms. We report the clinical and pathologic findings in

Severe hypoglycemia and hyponatremia caused by hypopituitarism in a female patient with type 1 diabetes: A case report.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

The misdiagnosis of hypopituitarism is common due to its rarity and its nonspecific clinical manifestations. Our case report highlights the importance of critical evaluation regarding hypopituitarism as a cause of recurrent hypoglycemia, hyponatremia, and gastrointestinal symptoms in

Swinging for the Fences: Long-Term Survival With Ipilimumab in Metastatic Melanoma.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

A 40-year-old man with stage III melanoma arising from his left shoulder underwent wide local excision, sentinel lymph node biopsy, and lymph node dissection. Nine months after receiving adjuvant biochemotherapy with cisplatin, vinblastine, dacarbazine, interleukin-2 (IL-2), and interferon alfa as

Renální toxicita imunoonkologické léčby.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Acute renal impairment is a relatively rare complication of anti-tumour immunotherapy. The incidence of renal toxicity due to immuno-oncological therapy is relatively low, approximately 2% in patients treated with PD-1/PD-L1 inhibitors and 4.5% with combination treatments with

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Herbal & Natural Medicine

המאגר השלם ביותר של צמחי מרפא המגובה על ידי המדע

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* כל המידע מבוסס על מחקר מדעי שפורסם

hypophysitis/בחילה

IgG4-related hypophysitis presenting as a pituitary adenoma with systemic disease.

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

Clinical course of a pituitary macroadenoma in the first trimester of pregnancy: probable lymphocytic hypophysitis.

A case of hypopituitarism associated with Hashimoto's thyroiditis and candidiasis: lymphocytic hypophysitis or Sheehan's syndrome?

Immunotherapy-induced autoimmune hypophysitis.

Idiopathic giant-cell granulomatous hypophysitis mimicking acute meningitis.

A Remarkable Response of Granulomatous Hypophysitis to Infliximab in a Patient With a Background of Crohn's Disease-A Case Report

Lymphocytic hypophysitis in a patient with systemic lupus erythematosus.

Granulomatous hypophysitis causing compression of the internal carotid arteries reversible with azathioprine and rituximab treatment.

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

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

Xanthomatous hypophysitis.

Severe hypoglycemia and hyponatremia caused by hypopituitarism in a female patient with type 1 diabetes: A case report.

Swinging for the Fences: Long-Term Survival With Ipilimumab in Metastatic Melanoma.

Renální toxicita imunoonkologické lé&#269;by.

המאגר השלם ביותר של צמחי מרפא המגובה על ידי המדע

Renální toxicita imunoonkologické léčby.