myxoma/hoofdpijn

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[Migrainous auras without cephalalgia in crescendo and optico-cerebral syndrome as clinical presentation of an atrial myxoma].

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Upper facial mass and headaches: think of myxoma.

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Rare association of acromegaly with left atrial myxoma in Carney's complex due to novel PRKAR1A mutation.

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Carney complex (CNC) is a rare autosomal dominant syndrome characterized by pigmented lesions of the skin and mucosae along with cardiac, endocrine, cutaneous, and neural myxomatous tumors. Mutations in the PRKAR1A gene have been identified in ∼70% of the CNC cases reported worldwide. A 30-year-old

Primary myxoma of the posterior fossa.

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A rare case of primary intracranial myxoma of the posterior fossa is described in a 32-year old woman. The patient presented with a history of headaches, disequilibrium, nausea and abnormal vision for several months. Computed tomography (CT) showed a well-demarcated hypodense mass. After contrast

[Polymyalgia syndrome and atrial myxoma].

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We present a case of polymyalgia-like syndrome in a 62-years-old woman with four month history of severe headache, muscular claudication, asthenia, normochromic, normocytic anaemia and elevation of erytrocyte sedimentation rate. A diagnosis of giant left atrial myxoma was made brought about by

[A case of cardiac myxoma presenting with multiple cerebellar hemorrhages and elevation of interleukin-6 in the cerebrospinal fluid].

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We report a 25-year old man with cardiac myxoma presenting with multiple cerebellar hemorrhages and elevation of interleukin-6 (IL-6) in the cerebrospinal fluid (CSF). The patient was first admitted to our hospital because of cerebral infarctions at the age of 23. After systemic exploration he was

Anesthesia management of atrial myxoma resection with multiple cerebral aneurysms: a case report and review of the literature

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Background: Embolic stroke is a common complication of atrial myxoma, whereas multiple cerebral aneurysms associated with atrial myxoma is rare. The pathogenesis of the cerebral vascular disease related to an atrial myxoma is still not

A rare aetiology of stroke; myxomatous aneurysm caused by atrial myxoma.

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Atrial myxoma is a rare cause of stroke. In this report we present the case of a 52-year-old female patient who went to hospital suffering from a headache. Her neurological examination was normal except for a positive Babinski sign on the left. In the superolateral of the right, a Sylvian fissure

Atrial myxoma with cerebellar signs: a case report.

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Atrial myxoma remains a rare clinical entity with an incidence of surgically resected cases of 0.5-0.7 per million population and prevalence of < 5 per 10,000. It typically manifests in woman after third decade of life; symptoms vary greatly and may present with arrhythmia,

Maxillary aggressive angiomyxoma showing ineffective to radiotherapy: a rare case report and review of literature.

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Aggressive angiomyxoma, mostly originating in the female pelvis and peritoneum or in the male analogous sites, is a rare mesenchymal neoplasm characterized with infiltrative growth to adjacent tissue and local recurrence after primary excision. Herein, we report a case of aggressive angiomyxoma of

Left atrial myoxma presenting as headache in the pediatric patient.

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BACKGROUND Cardiac myxomas rarely occur in children or adolescents. In addition, it is even more rare for the adolescent patient to present with neurological symptoms only. Early diagnosis is difficult because the symptoms of left atrial myxoma are frequently nonspecific. If delayed or left

[Myxoma of cranial base: study of 23 cases].

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OBJECTIVE To study the clinical manifestations and diagnosis and treatment of cranial base myxoma. METHODS The clinical data of 23 cases of myxoma of cranial base confirmed by pathology from Oct. 1983 to Nov. 2005, 14 males and 9 females, aged 32.7 (18 approximately 50), were analyzed

Orbital myxoma: A case report.

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Myxomas are rare, locally infiltrative, benign neoplasms of mesenchymal origin. Although benign, these tumors are locally aggressive with a high rate of recurrence following conservative resection. Their relative infrequency, variable location, and insidious growth present a diagnostic

Primary occipital myxoma: A rare case report.

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Myxomas are benign tumors arising from mesenchymal tissues throughout the body. These tumors are usually seen in the atrium of heart and the jaw bone. Only a few cases of primary intracranial myxomas have been described in the literature. A rare case of primary myxoma of the occipital region is

Primary intracranial myxoma of the parietal region. Illustrated case report.

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An extremely rare case of primary intracranial myxoma mimicking an intraaxial parenchymal tumour is reported. A 25 year old male presented with complaints of headache and right sided hemiparesis. A gross total resection of the tumour was achieved. Histology confirmed that the tumour was a myxoma.

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