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osteolysis/cefaleia
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Página 1 a partir de 18 resultados
Headache of a diagnosis: frontotemporal pain and inflammation associated with osteolysis.
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A 62-year-old woman presented with left frontotemporal pain, scalp tenderness and raised levels of inflammatory markers. Temporal arteritis was considered likely, and symptoms resolved with prednisone therapy. This delayed diagnostic bone biopsy until a soft tissue abscess formed, and Pott's puffy
Foramen magnum impaction in a case of acro-osteolysis.
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A case of a rare, non-familial, generalized, congenital, osseous dysplasia is described with features which have previously been described under the name 'acro-osteolysis'. Basilar invagination followed defective bone formation in the skull and this produced occipital headache and progressive
[Idiopathic massive osteolysis of skull bone: a case report].
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A rare case of idiopathic massive osteolysis of the skull is reported. A 49 year-old male was admitted with a diagnosis of a skull tumor. The skull film taken for evaluation of the headache, showed a large lytic lesion with irregular margin in the left parietal area. CT showed that some of the bone
Clinical and radiological investigations on cervical spine involvement in rheumatoid arthritis in adults.
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The radiological and clinical features of cervical spine involvement observed in 49 patients with rheumatoid arthritis are described. The forward atlas-odontoid subluxation, after an x-ray with full flexion of the cervical spine, occurred in 36.9% of the cases. The upward subluxation was found in 8
[An atypical presentation of primary cutaneous diffuse B-cell lymphoma, leg type].
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BACKGROUND
Primary cutaneous diffuse B-cell lymphoma, leg type, are rare and aggressive tumours frequently affecting elderly patients. We present a case of a 53-year-old woman with an atypical presentation of primary cutaneous diffuse B-cell lymphoma, leg type.
METHODS
Eight years after complete
Mastocytosis presenting as a skeletal disorder.
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Mastocytosis is a rare disease of mast-cell proliferation with involvement of the reticuloendothelial systems including skin, bone, gastrointestinal tract, liver, lungs, spleen, and lymph nodes. Systemic mastocytosis is characterized by a combination of symptoms that relate to the mast cells'
Nocardia nova sphenoid sinusitis and infratemporal fossa abscess.
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BACKGROUND
Nocardia sinusitis is exceptional, as a Medline search revealed only one published case. The authors report a case of sphenoid sinusitis complicated by infratemporal fossa abscess, which raised several diagnostic problems.
METHODS
The patient was referred with temporal headache, subacute
Multiple myeloma manifesting as an intraventricular brain tumor.
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Primary intracerebral manifestation of multiple myeloma is rare and usually arises from the meninges or brain parenchyma. The authors present a case of multiple myeloma primarily manifesting within the lateral ventricle. A 67-year-old man was admitted with headache accompanied by slowly progressing
Wegener's granulomatosis presenting as otomastoiditis. A case report.
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A 55-year-old male presented with left-sided otorrhoea, hearing loss and tinnitus of 3 months duration. On clinical examination polypoid tissue was seen prolapsing in the external ear canal. A CT scan of the mastoid cells and middle ear showed otomastoiditis with osteolysis. Oral antibiotic therapy
[The interesting case -- case no. 65].
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Bilateral Osteomyelitis following frontal sinusitis is a rare complication in the antibiotic era. The main risk of a progredient course is mainly the formation of external subperiostal, epidural, subdural abscesses or brain abscesses with potentially life-threatening complications. This is a report
Skull base chordomas: presentation of six cases and review of the literature.
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Chordomas are uncommon tumours occuring from remnants of the notochord. They are mainly localized in the sacrococcygium, the spine and the skull base. We focused our study on skull base chordomas and reviewed 531 published cases and 6 cases diagnosed in our institution. The six cases diagnosed at
Primary hyperparathyroidism on the example of a 33-year-old female patient with parathyroid adenoma
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Parathyroid hyperactivity is the state of over-production and PTH secretion [1]. The most common cause of primary hyperparathyroidism is parathyriod adenoma - about 80% of cases, the remaining are parathyroid hyperplasia around 15%cases [2] [3], and in 1-5% of cases, cancer [2] [3] [4] [5]. The
Complex single step skull reconstruction in Gorham's disease - a technical report and review of the literature.
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BACKGROUND
Gorham's disease is a rare osteolytic disorder characterized by progressive resorption of bone and replacement of osseous matrix by a proliferative non-neoplastic vascular or lymphatic tissue. A standardized treatment protocol has not yet been defined due to the unpredictable natural
Phytochemistry, pharmacological activities and uses of Indian traditional medicinal plant Kaempferia galanga L. - An overview.
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Primary calvarial meningioma.
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Primary intraosseous meningioma of the skull is uncommon. We report upon a 50-year-old male patient who presented with a history of an expanding scalp mass over a few months, associated with headache. The mass was initially misdiagnosed as congenital encephalocele. It was observed for 2 months, but
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