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osteoblastoma/back pain

Холбоосыг санах ойд хадгалдаг
НийтлэлЭмнэл зүйн туршилтПатент
Хуудас 1 -аас 38 үр дүн

Severe neck and back pain in adolescence: remember osteoblastoma.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
Osteoblastoma is a rare benign tumor of the bone. A 15-year-old boy presented with severe neck and back pain and was followed up for myofascial pain syndrome for 12 months. There was no neurologic deficit or scoliosis. The X-ray of the patient was normal. MRI revealed local destructive tumorous

Osteoblastoma of the lumbar spine as a cause of chronic low back pain.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
We report a case of osteoblastoma in the uncommon location of the L5 lumbar vertebra, detailing the clinical and radiologic aspects. Although the plain radiographs of the patient were normal, computed tomographic scans of the lumbar region confirmed the diagnosis of osteoblastoma or osteoid osteoma

Chronic Back Pain Diagnosed as Giant Osteoid Osteoma of the Thoracic Vertebra: A Case Report.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
Diagnosing an osteoid osteoma as a benign tumor can be challenging owing to its different presentation patterns, ambiguous radiological findings and unusual sites of involvement. The present case report involves a 30-year-old female patient with a large osteoid osteoma of the thoracic

Unusual cause of back pain in a 13-year-old boy: a thoracic osteoblastoma.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх

Osteoblastoma of the thoracic spine presenting with back pain.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх

Unusual presentation of osteoblastoma in a patient with idiopathic scoliosis after posterior spinal fusion.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
BACKGROUND Few studies have described the diagnosis of osteoblastoma of the spine as a cause of scoliosis. These reports have described the tumor in conjunction with initial presentation of painful scoliosis. This case report presents a case of osteoblastoma 9 years removed from diagnosis and fusion

Spinal osteoblastoma in children and adolescents.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
Osteoblastoma as a cause of back pain, scoliosis, and reversible neurological deficit has received scant attention in the neurosurgical literature. The tumor has a predeliction for the spine, occurs in young people, and may undergo sarcomatous change. Total removal is necessary for cure. Eight cases

[An unusual cause of secondary scoliosis: vertebral osteoblastoma].

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
We report the observation of a 22-year-old man suffering from nocturnal back pain for 2 years. The clinical examination shows a scoliosis. Imaging suggests either malignant tumor or an aggressive osteoblastoma of the sixth thoracic vertebra. After radical removal of the tumor, histopathologic

[Scoliosis of sudden evolution due to lumbar osteoblastoma].

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
The clinical presentation and treatment of a case of osteoblastoma of the lumbar spine (L4) is described, with a notable delay between the onset of symptoms and the definitive diagnosis (2 years). Besides scoliosis, the usual roentgenograms, bone scans, CAT and MRI, did not show any relevant

Osteoblastoma in lumbar vertebral body.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
We report a young man with low back pain suspected to have a disc protrusion. Imaging suggested a tumour of the dorsal portion of the fifth lumbar vertebral body. Operation suggested a giant-cell tumour and subsequent histology showed an osteoblastoma. All typical imaging features of osteoblastoma

Dorsal spine osteoblastoma.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
Benign osteoblastoma is a rare primary neoplasm comprising less than 1% of primary bone tumors.[1] We report a case of a 20-year-old female patient presenting with progressive paraparesis over one year and back pain over the dorsal spine gradually increasing in severity over a year. Computerised

Benign osteoblastoma of vertebral column and skull. Report of two cases.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
Osteoblastoma of the spine is a rare but important cause of back pain and the sciatica syndrome in young adults. Osteoblastoma of the skull is rare and the involvement of the orbital roof is very unusual. Clinical complaints and physical examination are not specific enough to provide a lead to the

Ossification of the ligamentum flavum associated with osteoblastoma: a report of three cases.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
We report three cases of spinal osteoblastoma with ossification of the ligamentum flavum (OLF) adjacent to the tumor. The patients in this report, all young adults, had no symptoms except for back pain. Computed tomography (CT) demonstrated a typical radiolucent nidus in the spinal pedicle/lamina

Vertebral osteoblastoma: are radiologic structural changes necessary for diagnosis?

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
BACKGROUND A case of osteoblastoma localized at the pedicle of the 10th thoracic vertebra is presented. METHODS The patient complained of nocturnal back pain not relieved by salycilates, a typical symptom of osteoblastoma. Bone scintigraphy showed a lower thoracic focus of increased osteoblastic

Lumbar extraosseous intraforaminal osteoblastoma: case report and review of the literature.

Зөвхөн бүртгэлтэй хэрэглэгчид л нийтлэл орчуулах боломжтой
Нэвтрэх / Бүртгүүлэх
Osteoblastomas are rare primary bone tumors with a predilection for the spine. The extraosseous growth pattern is rare: to our knowledge, only two cases of fully extraosseous osteoblastomas have been previously reported.A 36-year-old man presented with a
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