1.A Case of Primary Hepatocellular Carcinoma with Metastasis to The Spinal Cord.
Kwang Bum CHO ; Jung Ho SOHN ; Kyung Sik PARK ; Du Young KWON ; Young Soo LEE ; Jae Seok HWANG ; Jung Wook HUR ; Sung Hoon AHN ; Soong Kuk PARK
The Korean Journal of Hepatology 2002;8(2):218-222
Hepatocellular carcinoma is one of the most common malignancies reported in Korean adult males. Hepatocellular carcinoma usually spreads to regional lymph nodes around porta hepatis via lymphatics and to distant metastasis via hematogenous spread. The lung is most common distant metastatic site, followed by the adrenal glands, local lymph nodes and bones. But metastasis to the spinal cord of hepatocellular carcinoma is very rare. Recently we experienced a patient with hepatocellular carcinoma who had suffered from lower leg weakness for 10 days. The patient was proved to have hepatocellular carcinoma with metastasis to the spinal cord. MRI showed an ovoid intracordal mass between the twelfth thoracic and first lumbar vertebra level. After emergency irradiation, the patient could recover.
Carcinoma, Hepatocellular/*secondary
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English Abstract
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Human
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Liver Neoplasms/*pathology
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Magnetic Resonance Imaging
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Male
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Middle Aged
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Spinal Cord Neoplasms/diagnosis/*secondary
2.A Spinal Cord Astrocytoma and Its Concurrent Osteoblastic Metastases at the Time of the Initial Diagnosis: a Case Report and Literature Review.
Ah Young PARK ; Hyunki KIM ; Tae Sub CHUNG ; Choon Sik YOON ; Young Hoon RYU ; Yong Eun CHO ; Eun Su MOON ; Sungjun KIM
Korean Journal of Radiology 2011;12(5):620-625
Bone metastasis from a spinal cord astrocytoma has been reported only twice in the English medical literature. It is generally known that bone metastasis is found after the initial diagnosis with/without intervening surgery rather than being found at the time of the diagnosis of astrocytoma. The purpose of this article is to report for the first time a case of concurrent bone metastasis from a spinal cord astrocytoma at the time of diagnosing the spinal cord astrocytoma.
Astrocytoma/diagnosis/*secondary
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Humans
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*Lumbar Vertebrae
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Magnetic Resonance Imaging
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Male
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Middle Aged
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Spinal Cord Neoplasms/diagnosis/*pathology
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Spinal Neoplasms/diagnosis/*secondary
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*Thoracic Vertebrae
3.Brown Tumor of the Thoracic Spine: First Manifestation of Primary Hyperparathyroidism.
Erkin SONMEZ ; Tugan TEZCANER ; Ilker COVEN ; Aysen TERZI
Journal of Korean Neurosurgical Society 2015;58(4):389-392
Brown tumors also called as osteoclastomas, are rare nonneoplastic lesions that arise in the setting of primary or secondary hyperparathyroidism. Parathyroid adenomas or hyperplasia constitute the major Brown tumor source in primary hyperparathyroidism while chronic renal failure is the leading cause in secondary hyperparathyroidism. Most of the patients with the diagnosis of primary hyperparathyroidism present with kidney stones or isolated hypercalcemia. However, nearly one third of patients are asymptomatic and hypercalcemia is found incidentally. Skeletal involvement such as generalized osteopenia, bone resorption, bone cysts and Brown tumors are seen on the late phase of hyperparathyroidism. The symptoms include axial pain, radiculopathy, myelopathy and myeloradiculopathy according to their locations. Plasmocytoma, lymphoma, giant cell tumors and metastates should be ruled out in the differential diagnosis of Brown tumors. Treatment of Brown tumors involve both the management of hyperparathyroidism and neural decompression. The authors report a very rare spinal Brown tumor case, arisen as the initial manifestation of primary hyperparathyroidism that leads to acute paraparesis.
Bone Cysts
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Bone Diseases, Metabolic
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Bone Resorption
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Decompression
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Diagnosis
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Diagnosis, Differential
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Giant Cell Tumors
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Humans
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Hypercalcemia
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Hyperparathyroidism
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Hyperparathyroidism, Primary*
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Hyperparathyroidism, Secondary
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Hyperplasia
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Kidney Calculi
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Kidney Failure, Chronic
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Lymphoma
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Paraparesis
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Parathyroid Neoplasms
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Plasmacytoma
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Radiculopathy
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Spinal Cord Diseases
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Spine*
4.MR imaging of meningeal carcinomatosis by systemic malignancy.
Lin MA ; Shengyuan YU ; Youquan CAI ; Li LIANG ; Xinggao GUO
Chinese Medical Sciences Journal 2003;18(1):36-40
OBJECTIVETo investigate the magnetic resonance (MR) features of meningeal carcinomatosis, and to improve the ability in understanding and diagnosing meningeal carcinomatosis by MR findings.
METHODSEleven cases with proven meningeal carcinomatosis were studied by conventional and Gd-DTPA enhanced MR imaging. The enhancement patterns and features, as well as the types of meningeal involvement, were retrospectively analyzed.
RESULTSConventional MR imaging showed no evident meningeal abnormalities. After the administration of Gd-DTPA, abnormal pia mater enhancement was detected in 9 cases, demonstrating as the continuous, thin, and lineal high signal intensity on the brain surface that could descend into the sulci. The abnormal pial enhancement occurred on the cortical surfaces of cerebellum, brainstem, and cerebrum. No abnormal enhancement in the subarachnoid space was found. Abnormal dura-arachnoid enhancement was seen in 3 cases, showing as the continuous, thick, and curvilineal high signal intensity over the convexities or in the tentorium without extension into the cortical sulci. Cerebral dura-arachnoid involvement was found in all 3 cases and one of them also showed abnormal enhancement in cerebellar dura-arachnoid and tentorium. Of the 11 cases, 9 with pial involvement had abnormal cerebrospinal fluid (CSF) results, 2 involving only the dura-arachnoid had normal CSF results.
CONCLUSIONMeningeal carcinomatosis could be well demonstrated by Gd-DTPA enhanced MR imaging, and its type could be differentiated by the enhancement features. Combined with the clinical information, Gd-enhanced MR imaging may lead to the diagnosis and guide the therapy of meningeal carcinomatosis.
Adolescent ; Adult ; Aged ; Breast Neoplasms ; pathology ; Child ; Contrast Media ; Female ; Gadolinium DTPA ; Humans ; Image Enhancement ; Lung Neoplasms ; pathology ; Magnetic Resonance Imaging ; Male ; Meningeal Neoplasms ; diagnosis ; secondary ; Middle Aged ; Precursor Cell Lymphoblastic Leukemia-Lymphoma ; pathology ; Retrospective Studies ; Spinal Cord Neoplasms ; diagnosis ; secondary
5.Spinal cord injury after conducting transcatheter arterial chemoembolization for costal metastasis of hepatocellular carcinoma.
Sang Jung PARK ; Chang Ha KIM ; Jin Dong KIM ; Soon Ho UM ; Sun Young YIM ; Min Ho SEO ; Dae In LEE ; Jun Hyuk KANG ; Bora KEUM ; Yong Sik KIM
Clinical and Molecular Hepatology 2012;18(3):316-320
Transcatheter arterial chemoembolization (TACE) has been used widely to treat patients with unresectable hepatocellular carcinoma. However, this method can induce various adverse events caused by necrosis of the tumor itself or damage to nontumor tissues. In particular, neurologic side effects such as cerebral infarction and paraplegia, although rare, may cause severe sequelae and permanent disability. Detailed information regarding the treatment process and prognosis associated with this procedure is not yet available. We experienced a case of paraplegia that occurred after conducting TACE through the intercostal artery to treat hepatocellular carcinoma that had metastasized to the rib. In this case, TACE was attempted to relieve severe bone pain, which had persisted even after palliative radiotherapy. A sudden impairment of sensory and motor functions after TACE developed in the trunk below the level of the sternum and in both lower extremities. The patient subsequently received steroid pulse therapy along with supportive care and continuous rehabilitation. At the time of discharge the patient had recovered sufficiently to enable him to walk by himself, although some paresthesia and spasticity remained.
Antiviral Agents/therapeutic use
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Bone Neoplasms/radiography/secondary
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Carcinoma, Hepatocellular/diagnosis/pathology/*therapy
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Catheter Ablation
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Chemoembolization, Therapeutic/*adverse effects
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Hepatitis B/complications/drug therapy
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Humans
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Liver Cirrhosis/etiology
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Liver Neoplasms/diagnosis/pathology/*therapy
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Male
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Middle Aged
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Positron-Emission Tomography
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Soft Tissue Neoplasms/secondary
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Spinal Cord Injuries/*etiology
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Tomography, X-Ray Computed
6.Intramedullary Spinal Cord Metastasis in Renal Cell Carcinoma: A Case Report of the Surgical Experience.
Jeongill PARK ; Seok Won CHUNG ; Kyoung Tae KIM ; Dae Chul CHO ; Jeong Hyun HWANG ; Joo Kyung SUNG ; Dakeun LEE
Journal of Korean Medical Science 2013;28(8):1253-1256
Intramedullary spinal cord metastasis (ISCM) from renal cell carcinoma (RCC) is rare manifestation and most of them are treated by adjuvant treatment modalities like radiotherapy. Despite the radio-resistance of RCC itself, focal radiotherapy has been preferred as the first-line treatment modality of ISCM from RCC and only a few cases underwent surgical treatment. We describe a case of ISCM from RCC, which underwent surgical excision and pathologically confirmed. A 44-yr-old man was presented with rapid deterioration of motor weakness during focal radiotherapy for ISCM from RCC. After the surgery for removal of the tumor mass and spinal cord decompression, his motor power was dramatically improved to ambulate by himself. We report the first published Korean case of ISCM from RCC confirmed pathologically and describe our surgical experience and his clinical characteristics.
Adult
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Carcinoma, Renal Cell/*diagnosis/pathology/surgery
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Humans
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Immunohistochemistry
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Keratins/metabolism
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Magnetic Resonance Imaging
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Male
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Motor Activity/physiology
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Spinal Cord Neoplasms/pathology/secondary/*surgery
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Tomography, X-Ray Computed
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Treatment Outcome
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Vimentin/metabolism