neurofibromatoses/bjúgur

Krækjan er vistuð á klemmuspjaldið

Veldu tegund tegund

Bls 1 frá 75 niðurstöður

Lymphangiopathy in neurofibromatosis 1 manifesting with chylothorax, pericardial effusion, and leg edema.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

BACKGROUND This case report documents the affliction of the lymph vessels as a phenotypic feature of neurofibromatosis-1 (NF-1). METHODS Routine transthoracic echocardiography, computed tomography scan of the thorax, magnetic resonance angiography of the renal arteries, and conventional digital

Intravitreal bevacizumab role in the treatment of macular edema secondary to retinal vasoproliferative tumor in a patient with neurofibromatosis type 1.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

Objective: To report a case of neurofibromatosis-1 (NF-1) with retinal vasoproliferative tumor (RVPT) and macular edema and exudation that was successfully treated with intravitreal bevacizumab (IVB). Method: A retrospective case report of patient with neurofibromatosis, retinal vasoproliferative

Severe optic disc edema without hydrocephalus in neurofibromatosis 2.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

A 26-year-old man who had neurofibromatosis type-2 with symptoms of unexplained optic disc edema is reported. Magnetic resonance imaging (MRI) revealed bilateral acoustic schwannomas. Obstructive hydrocephalus, however, was not evident in spite of his severe disc edema and visual loss. After partial

Optic nerve glioma and cerebellar astrocytoma in a patient with von Recklinghausen's neurofibromatosis.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

A 2 and a half year-old boy with neurofibromatosis developed unilateral proptosis, decreased visual acuity, and optic disk edema. After the discovery and removal of an optic nerve glioma, the patient had ten years of excellent health until he began having headaches, nausea, and vomiting. He had

[Myxedema coma in a patient with type 1 neurofibromatosis: rare association].

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

Myxedema coma, a rare but fatal emergency, is an extreme expression of hypothyroidism. We describe a 51-year-old male patient who has discontinued hypothyroidism treatment 10 months earlier and developed lethargy, edema, and cold intolerance symptoms. He also had a previous diagnosis of

Branch retinal vein occlusion in a Japanese patient with neurofibromatosis 1.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

BACKGROUND To report an Asian patient with branch retinal vein occlusion secondary to neurofibromatosis 1. METHODS A 64-year-old woman presented with a loss of vision in her right eye of 9-month duration. A diagnosis of neurofibromatosis 1 was made. A general medical examination showed no

A rare case of sudden death due to hypotension during cesarean section in a woman suffering from pheochromocytoma and neurofibromatosis.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

Sudden death following acute hypotension due to an undiagnosed pheochromocytoma (PHEO) is a rare event. Moreover, histopathology of the myocardium in such cases is rarely reported. We present a case of a woman who died during delivery. A 37-year-old parturient, who was 38 weeks pregnant, suffering

Atypical hematologic and renal manifestations in neurofibromatosis type I: coincidence or pathophysiological link?

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

Neurofibromatosis type 1 (NF1) is an autosomal dominant, multi-system, neurocutaneous disorder that predisposes to the development of benign and malignant tumors with a birth incidence rate of 1 in 2500-3000. 50% of cases are sporadic. The diagnosis is exclusively based on clinical assessment with

Acute myocardial infarction attributable to adrenergic crises in a patient with pheochromocytoma and neurofibromatosis 1.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

OBJECTIVE To describe a rare case of acute myocardial infarction in a patient with neurofibromatosis 1 and pheochromocytoma and to review the literature on the coexistence of these 2 diseases, the causes of myocardial injury in patients with pheochromocytoma, and the utility of genetic testing and

Is magnetic resonance spectroscopy capable of detecting metabolic abnormalities in neurofibromatosis type 1 that are not revealed in brain parenchyma of normal appearance?

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

BACKGROUND Results of magnetic resonance spectroscopy studies in normal-appearing brain and in non-neoplastic brain lesions in individuals with neurofibromatosis type 1 (NF1) have been discrepant. OBJECTIVE We used magnetic resonance spectroscopy to analyze the metabolic patterns in the basal

Laser interstitial thermotherapy for treatment of symptomatic peritumoral edema after radiosurgery for meningioma.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

Symptomatic peritumoral edema (PTE) is a known complication following radiosurgical treatment of meningiomas. While the edema in most patients can be successfully managed conservatively with corticosteroid therapy or bevacizumab, some medically refractory cases may require surgical

High-intensity basal ganglia lesions on T1-weighted MR images in neurofibromatosis.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

Basal ganglia lesions, characterized on MR by increased signal intensity on T1-weighted images, were observed in seven patients with documented neurofibromatosis. These lesions most often involved the globus pallidus and internal capsules in a bilateral and symmetric fashion, and extended across the

High-intensity basal ganglia lesions on T1-weighted MR images in neurofibromatosis.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

Validation of a Scoring System to Evaluate the Risk of Rapid Growth of Intracranial Meningiomas in Neurofibromatosis Type 2 Patients

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

Objective: Intracranial meningiomas occur in about half of neurofibromatosis type 2 (NF2) patients and are very frequently multiple. Thus, estimating individual meningiomas' growth rates is of great interest to tailor therapeutic interventions. The Asan

A rare case of neurofibromatosis - type 1.

Aðeins skráðir notendur geta þýtt greinar

Skráðu þig / skráðu þig

Neurofibromatosis type 1 (NF1), also known as von Recklinghausen disease, is an autosomal dominant familial tumor syndrome. Glioblastoma is a malignant brain tumor but is a rare occurrence in patients with NF1. Here, we report a rare occurrence of glioblastoma in a 60-year-old man with NF1, who

Fyrri
1
2
3
4
5
Næst

Skráðu þig á
facebook síðu okkar

Herbal & Natural Medicine

Heillasta gagnagrunnur lækningajurtanna sem studdur er af vísindum

Virkar á 55 tungumálum
Jurtalækningar studdir af vísindum
Jurtaviðurkenning eftir ímynd
Gagnvirkt GPS kort - merktu jurtir á staðsetningu (kemur fljótlega)
Lestu vísindarit sem tengjast leit þinni
Leitaðu að lækningajurtum eftir áhrifum þeirra
Skipuleggðu áhugamál þitt og vertu vakandi með fréttarannsóknum, klínískum rannsóknum og einkaleyfum

Sláðu inn einkenni eða sjúkdóm og lestu um jurtir sem gætu hjálpað, sláðu jurt og sjáðu sjúkdóma og einkenni sem hún er notuð við.
* Allar upplýsingar eru byggðar á birtum vísindarannsóknum