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hemangiosarcoma/כאב ראש

הקישור נשמר בלוח
מאמריםניסויים קלינייםפטנטים
עמוד 1 מ 20 תוצאות

Clinical and pharmacologic evaluation of two dose levels of intetumumab (CNTO 95) in patients with melanoma or angiosarcoma.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
OBJECTIVE In this Phase 1, multicenter, open-label study, intetumumab (CNTO 95), a fully human anti-αv integrin monoclonal antibody was evaluated for safety, pharmacokinetics, and pharmacodynamic activity in patients with melanoma or angiosarcoma. METHODS Patients with histologically-confirmed

Metastatic angiosarcoma of the brain.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Two patients with metastatic angiosarcoma of the brain are described. In one, a 17-year-old man, the tumor was located at the pineal region and exhibited significant vascularity. It was sensitive to radiation therapy and disappeared after radiation of 50 Gy; however, it recurred after 1 year and a

Therapeutic options for primary meningeal angiosarcoma: A case report

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Background: Primary angiosarcoma (AS) of the central nervous system (PACNS) is an extremely rare malignancy. The meninges represent an uncommon site of origin of PACNS. This report describes a recurrent meningeal PACNS treated with

[A case of nasal big angiosarcoma].

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Angiosarcoma also called malignant hemangioendothelioma, caused by vascular endothelial cells or in the direction of vascular endothelial cell differertiation of mesenchymal malignant tumor, is a rare tumor found in clinical, can be in any place of the body, such as head and neck, skin and tissue,

Rapid clinical course of cerebral metastatic angiosarcoma from the heart.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
We report here one case of rapid and aggressive course of cerebral metastatic angiosarcoma from the heart. A 36-year-old man presented with 10-days history of headache. Magnetic resonance imaging demonstrated subacute hemorrhage with a small region of enhancement in right parietal region and the

[Angiosarcoma of the liver and pineal region].

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Angiosarcoma is a rare malignant tumor originating from vascular endothelial cells. We have experienced a case of 17-year-old man, who had angiosarcoma in the pineal region and the liver. Patient's initial symptom was headache and CT scan revealed a high density mass in the pineal region with

Primary cerebellopontine angle angiosarcoma.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Primary intracranial angiosarcomas are rare. Only a few cases have been reported in the literature. All cases reported were located in the supratentorial areas. To our knowledge, no cerebellopontine (CP) angle angiosarcoma has been reported. We report a 16-year-old girl who had mild headache,

[A case of angiosarcoma of the heart with cardiac tamponade and repeated hemoptysis].

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
A 30-year-old man who died from brain metastasis of cardiac angiosarcoma is presented. His chest X-ray film showed cardiac tamponade and bilateral pleural effusion. His symptoms were improved only by drainage of the bloody pericardial and pleural effusion. During the course of the disease, multiple

A rare case of primary breast angiosarcoma in a male: a case report.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
BACKGROUND Sarcomas account for less than 1% of primary breast cancers, and breast angiosarcomas are responsible for only 0.05% of all breast malignancies. The male breast has the same potential for malignant transformation as the female breast. However, due to anatomical differences in the breast

Case 213: primary splenic angiosarcoma.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
History A 75-year-old woman with a medical history of gastroesophageal reflux disease and type II diabetes presented to the hospital with a 3-month history of gradually worsening headaches, vague upper abdominal pain, and lower back pain. The patient denied fevers, night sweats, contact with sick

Spindle cell hemangioma of the spleen: A case report.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Spindle cell hemangioma (SCH) is considered a benign vascular lesion. It typically develops as a solitary nodule or multiple masses located in the dermal or subcutaneous layers of the distal extremities. To the best of our knowledge, there are no prior reports of SCH in the

Nasopharyngeal undifferentiated carcinoma with sarcomatoid features: Pitfalls in the immunohistochemistry.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
We present a case of an undifferentiated subtype of non-keratinizing squamous cell carcinoma (NK-SCC) with sarcomatoid features in the nasopharynx in a 69-year-old man who was difficult to diagnose due to spindle-shaped malignant cells. He was admitted because of a right nasal obstruction and right

Tumour bleed manifesting as spontaneous extradural haematoma in posterior fossa.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
We report a unique case of primary extradural angiosarcoma of posterior fossa manifesting as extradural haematoma in a 12-year-old boy who presented with acute onset headache, vomiting, nuchal rigidity and altered sensorium. The patient underwent a retromastoid suboccipital craniotomy on emergency

Assessment of emergency responders after a vinyl chloride release from a train derailment - New Jersey, 2012.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
On November 30, 2012, at approximately 7:00 am, a freight train derailed near a small town in New Jersey. Four tank cars, including a breached tank car carrying vinyl chloride, landed in a tidal creek. Vinyl chloride, a colorless gas with a mild, sweet odor, is used in plastics manufacture. Acute

A case of retiform-hemangioendothelioma with unusual presentation and aggressive clinical features.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Retiform hemangioendothelioma (RH) is an extremely rare low-grade angiosarcoma mainly involving the skin and subcutaneous tissue. Clinically patients often present with an asymptomatic slow-growing solitary nodular or plaque-like lesion. RH is characterized by frequent local recurrences but a very
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