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Status of Photovoltaics in the world (2008년 세계 태양광발전산업 현황)

  • Yu, Gwon-Jong;Kang, Gi-Hwan;Park, Kyung-Eun;Kim, Hyun-Il;Kim, Jun-Tae
    • Proceedings of the KIEE Conference
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    • 2009.07a
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    • pp.1088_1089
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    • 2009
  • The photovoltaic(PV) industry has been growing worldwide. Recently, the PV industries not also in the traditional PV advanced countries but also in other countries are rapidly growing. Especially, China has become the largest supplier in the world PV supply side since 2007. Both the world PV supply and demand rose steadily in 2008 like recent bumper years. In 2008, the world solar cell production reached 6.85GW~7.91GW presenting growth of 85% over the previous year. On the demand side, 81 countries contributed to the 5.95GW presenting growth of 110% over the previous year.

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Thyroid Carcinoma Presenting as Hot nodule on Technetium-99m Pertechnetate Thyroid Scintigraphy (Technetium-99m Pertechnetate 갑상선 스캔에서 열결절로 나타난 갑상선암)

  • Shong, Young-Kee;Lee, Mun-Ho;Ryu, Jin-Sook;Moon, Dae-Hyuk;Lee, Myung-Hae
    • The Korean Journal of Nuclear Medicine
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    • v.26 no.1
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    • pp.147-150
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    • 1992
  • In general, hot nodules on techetium scan are regarded as benign tumors, and usually no further work up for malignancy is indicated, if they are truly autonomous. The authors experienced two cases of thyroid carcinoma presenting as hot nodule on technetium-99m pertechnetate thyroid scintigraphy. One case with papillary carcinoma, and other case with follicular carcinoma are presented in addition to a review of the literature.

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Bilateral Nephromegaly as a Presenting Symptom of Acute Lymphoblastic Leukemia (양측 신장비대로 진단된 급성림프구성 백혈병 1례)

  • Kim, Jong-Ho;Park, Jee-Min;Jung, Hyun-Joo;Park, Jun-Eun;Pai, Ki-Soo
    • Childhood Kidney Diseases
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    • v.13 no.2
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    • pp.278-281
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    • 2009
  • Bilateral renal enlargement is a very rare manifestation as the primary presenting feature of acute lymphoblastic leukemia. We are reporting an unusual clinical picture of a 9-month-old male patient diagnosed as precusor B-cell lymphoblastic leukemia, who showed bilateral nephromegaly without any hepatosplenomegaly at the time of initial presentation.

A Case of Vascular Leiomyoma Presenting as a Soft Mass of the Hard Palate (경구개 연성종물로 발현된 혈관평활근종 1예)

  • Yoon, Tae-Mi;Jung, Ki-Hong;Yang, Hyung-Chae;Lee, Joon-Kyoo
    • Korean Journal of Head & Neck Oncology
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    • v.26 no.2
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    • pp.250-252
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    • 2010
  • Vascular leiomyomas are benign tumors of smooth muscle origin arising from the muscularis layer of blood vessel walls. They can occur anywhere in the body where smooth muscle is found and usually occur in the lower extremity as a slow-growing, firm, occasionally painful mass. However they are rare in the head and neck and very rare in hard palate. Here we report a case of a vascular leiomyoma presenting as a soft mass of the hard palate and review the literatures.

Thyroid Papillary Carcinoma Presenting as Posterior Pharyngeal Mass : A Case Report (후인두 종물로 나타난 갑상선 유두상 암종 1예)

  • Kang, Jae-Ho;Yang, Si-Chang;Kim, Choon-Dong;Kim, Seung-Woo
    • Korean Journal of Head & Neck Oncology
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    • v.26 no.2
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    • pp.221-224
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    • 2010
  • Papillary thyroid carcinoma frequently invades the lymph node, trachea, esophagus and perithyroid tissue. However, direct extension to posterior pharyngeal area is known to be rare. A 64-year-old male was referred to our clinic presenting as posterior pharyngeal mass during gastrofiberscopy. The neck CT scan showed soft tissue mass in retropharynx and lymph node in right level III with calcifications. We performed the total thyroidectomy with selective(level II, III, IV) and anterior compartment neck dissection. In operative findings, the right thyroid mass were connected to the retropharynx through the posterior portion of inferior constrictor muscle. Histopathologic findings revealed the papillary thyroid carcinoma extended to retropharynx. We report a unique case with a literature review.

Pituitary Apoplexy Presenting as Isolated Oculomotor Nerve Palsy

  • Yang, Moon-Seok;Cho, Won-Ho;Cha, Seung-Heon
    • Journal of Korean Neurosurgical Society
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    • v.41 no.4
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    • pp.246-247
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    • 2007
  • The most common cause of isolated oculomotor nerve palsy is ischemia of the peripheral nerve caused by a disease, such as diabetes mellitus. Another common cause of isolated oculomotor nerve palsy is compression by an intracranial aneurysm, usually an posterior communicating artery aneurysm. However, it is extremely rare in the pituitary tumor. We report an unusual case of pituitary adenoma presenting with isolated oculomotor nerve palsy in the setting of pituitary apoplexy. We suggest that pituitary apoplexy should be included in the differential diagnosis of a patient with isolated oculomotor nerve palsy and early surgery should be considered for preservation of oculomotor nerve function.

Progressively Enlarged Intracerebral Ependymal Cyst Presenting with Movement Disorder

  • Lee, Seong-Jun;Hong, Chang-Ki;Ahn, Jung-Yong;Lee, Kyu-Sung
    • Journal of Korean Neurosurgical Society
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    • v.41 no.4
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    • pp.252-254
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    • 2007
  • Ependymal cysts are neuroepithelial cysts, typically found in the central white matter of the temporoparietal and frontal lobes. Clinical symptoms usually result from neurological deficits referable to these regions, from seizures, and chronic headaches associated with increased intracranial pressure. We describe here a case of ependymal cyst on the right fronto-parietal lobe, presenting with tremor and weakness. The cyst was resected surgically and presurgical neurological abnormalities were improved. An exploratory surgery with establishment of an adequate route of drainage and histological examination of the cyst wall are mandatory in the management of patients with a progressive and symptomatic intraparenchymal cyst.

Intracranial Chronic Subdural Hematoma Presenting with Intractable Headache after Cervical Epidural Steroid Injection

  • Kim, Myungsoo;Park, Ki-Su
    • Journal of Korean Neurosurgical Society
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    • v.58 no.2
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    • pp.144-146
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    • 2015
  • Postdural punctural headache (PDPH) following spinal anesthesia is due to intracranial hypotension caused by cerebrospinal fluid (CSF) leakage, and it is occasionally accompanied by an intracranial hematoma. To the best of our knowledge, an intracranial chronic subdural hematoma (CSDH) presenting with an intractable headache after a cervical epidural steroid injection (ESI) has not been reported. A 39-year-old woman without any history of trauma underwent a cervical ESI for a herniated nucleus pulposus at the C5-6 level. One month later, she presented with a severe headache that was not relieved by analgesic medication, which changed in character from being positional to non-positional during the preceding month. Brain magnetic resonance imaging revealed a CSDH along the left convexity. Emergency burr-hole drainage was performed and the headache abated. This report indicates that an intracranial CSDH should be considered a possible complication after ESI. In addition, the event of an intractable and changing PDPH after ESI suggests further evaluation for diagnosis of an intracranial hematoma.

Acute Spinal Subdural Hematoma Presenting with Spontaneously Resolving Hemiplegia

  • Oh, Seung-Hun;Han, In-Bo;Koo, Young-Ho;Kim, Ok-Joon
    • Journal of Korean Neurosurgical Society
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    • v.45 no.6
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    • pp.390-393
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    • 2009
  • Although prompt diagnosis and emergent surgical intervention are important in acute spinal subdural hematoma (SSDH), some cases with spontaneous remission of symptom and hematoma without surgery have been reported. We present a case of acute nontraumatic SSDH presenting with transient left hemiplegia for 4 hours. A magnetic resonance imaging study of cervical spine confirmed SSDH with C3-6 cervical cord compression at the left side. The patient had conservative management without recurrence. Although hemiplegia is an unusual clinical manifestation of SSDH, it should be differentiated from that of cerebrovascular origin promptly. Conservative management may be an alternative therapeutic option for selective cases with transient neurological deficits.

Macroprolactinoma in a young man presenting with erectile dysfunction

  • Song, Seung-Hun;Lee, Jinil;Kim, Dong Suk
    • Clinical and Experimental Reproductive Medicine
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    • v.46 no.4
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    • pp.202-205
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    • 2019
  • Hyperprolactinemia due to a pituitary adenoma is a rare cause of erectile dysfunction (ED). The prevalence of clinically apparent prolactinomas is reported to be from 6-10 to 50 per 100,000. A few reports have been published of prolactinoma presenting with ED. Here, we report a rare case of a young man who presented with ED as a chief complaint and who was diagnosed with a huge prolactinoma, and we discuss a related fertility issue.