mastocytosis/отёк

Ссылка сохраняется в буфер обмена

СтатьиКлинические испытанияПатенты

Выберите тип сортировки

Страница 1 от 30 полученные результаты

Exophthalmos, Diplopia, and Bilateral Eyelid Edema: Symptoms of Ocular Mastocytosis.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

Mastocytosis is characterized by clonal mast cell proliferation with accumulation within various organs and uncontrolled activation with excessive mast cell mediator release. Ocular manifestations have rarely been published. We describe a 63-year-old man with bilateral exophthalmos that led to the

Spontaneous antenatal resolution of canine hydrops fetalis diagnosed by ultrasound.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

A previously unreported syndrome of transient mid-gestational hydrops fetalis identified by ultrasound was diagnosed in 16 litters of 16 different dogs between November 1999 and May 2002. During this study period, a total of 161 canine pregnancies were diagnosed by ultrasound. A 17th litter of eight

[Recurrent syncope as a presenting symptom of systemic mastocytosis].

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

A 48-year-old man presented with recurrent syncope which was preceded by facial edema and difficulty in breathing. Physical examination, laboratory tests, abdominal CT and bone scan were all within normal limits. Bone marrow biopsy was consistent with mastocytosis. Systemic mastocytosis consists of

[Colonic involvement in systemic mastocytosis (author's transl)].

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

The most common gastrointestinal lesions encountered in systemic mastocytosis are the gastric, duodenal and small bowell lesions. The authors present a case of diffuse colonic involvement diagnosed on a double contrast examination. The radiological signs correlated with the endoscopical and

Renal involvement and favorable outcome in a child with mastocytosis

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

Mastocytosis is a rare myeloproliferative disease in which mast cells abnormally accumulate in the skin, bone marrow, intestine, liver, spleen, and lymph nodes. Characterized by uncontrolled proliferation of aberrant mast cells, the disease can present either cutaneously or systemically. Mast cells

Intrahepatic cholestasis due to systemic mastocytosis: a case report and review of literature.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

A 35-yr-old female presented with symptoms of obstructive jaundice. Liver biopsy, bone marrow aspiration, and biopsy revealed systemic mastocytosis and acute myeloid leukemia. The liver biopsy specimen showed infiltration of mast cells within portal tracts with periductal and portal edema,

Tetany, malabsorption, and mastocytosis.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

Mastocytosis is characterized by increased proliferation of mast cells. Two patients had systemic mastocytosis involving the skin and gastrointestinal tract, complicated by malabsorption and tetany. Absorption studies in these patients suggested that the entire small bowel was involved and that the

Systemic mastocytosis in 16 dogs.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

The clinical and pathologic features of systemic mastocytosis in 16 dogs are reported. There was no apparent breed or sex predilection, and the median age at presentation was 9.5 years. In 14 of 16 cases there was a primary cutaneous mast cell tumor (MCT). When cutaneous tumor location was compared

[Systemic mast cell disease associated with cutaneous xanthomas and markedly elevated serum IgE].

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

Systemic mast cell disease (SMCD) is a rare disease often associated with symptoms of general malaise, pruritus, diarrhea, vomiting, fever, urticaria pigmentosa, hepatosplenomegaly and lymphadenopathy. We reported a case of SMCD associated with cutaneous xanthoma and serum hyper IgE. Skin biopsy

Pulmonary mastocytosis and enhanced lung inflammation in mice heterozygous null for the Foxf1 gene.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

The Forkhead Box f1 (Foxf1) transcriptional factor (previously known as HFH-8 or Freac-1) is expressed in endothelial and smooth muscle cells in the embryonic and adult lung. To assess effects of Foxf1 during lung injury, we used CCl(4) and butylated hydroxytoluene (BHT) injury models. Foxf1(+/-)

The care pathway for children with urticaria, angioedema, mastocytosis.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

Cutaneous involvement characterized by urticarial lesions with or without angioedema and itch is commonly observed in routine medical practice. The clinical approach may still remain complex in real life, because several diseases may display similar cutaneous manifestations. Urticaria is a common

Novel approaches to treating advanced systemic mastocytosis.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

Mastocytosis is a myeloproliferative neoplasm characterized by expansion of abnormal mast cells (MCs) in various tissues, including skin, bone marrow, gastrointestinal tract, liver, spleen, or lymph nodes. Subtypes include indolent systemic mastocytosis, smoldering systemic mastocytosis and advanced

Masitinib for the treatment of systemic and cutaneous mastocytosis with handicap: a phase 2a study.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

Treatment options for patients suffering from indolent forms of mastocytosis remain inadequate with the hyperactivation of mast cells responsible for many of the disease's systemic manifestations. Masitinib is a potent and highly selective oral tyrosine kinase inhibitor. A combined inhibition of

A case of POEMS syndrome associated with essential thrombocythaemia and dermal mastocytosis.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

We describe a case of POEMS syndrome presenting with the recognized features of polyneuropathy, organomegaly, endocrine abnormalities, monoclonal protein, skin changes and anasarca. The patient was found to have both a solitary sclerotic plasmacytoma of the pelvis and evidence of Castleman's disease

Idiopathic Anaphylaxis: A Form of Mast Cell Activation Syndrome.

Только зарегистрированные пользователи могут переводить статьи

Войти Зарегистрироваться

Idiopathic anaphylaxis is a condition caused by paroxysmal episodes of sudden-onset multiorgan involvement variably including laryngeal edema, urticaria, bronchoconstriction, dyspnea, hypoxia, abdominal pain, nausea, vomiting, diarrhea, and hypotension. Rarely, the episodes can lead to

Присоединяйтесь к нашей
странице facebook

Herbal & Natural Medicine

Самая полная база данных о лекарственных травах, подтвержденная наукой

Работает на 55 языках
Травяные лекарства, подтвержденные наукой
Распознавание трав по изображению
Интерактивная карта GPS - отметьте травы на месте (скоро)
Прочтите научные публикации, связанные с вашим поиском
Ищите лекарственные травы по их действию
Организуйте свои интересы и будьте в курсе новостей исследований, клинических испытаний и патентов

Введите симптом или заболевание и прочтите о травах, которые могут помочь, введите лекарство и узнайте о болезнях и симптомах, против которых оно применяется.
* Вся информация основана на опубликованных научных исследованиях.