• Title/Summary/Keyword: Uncommon location

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Myofibroblastic sarcoma of the mandible: a case report

  • Park, Kyung-Ran;Jang, Hyo-Won;Won, Ji-Hoon;Kim, Hyun-Sil;Cha, In-Ho;Kim, Hyung-Jun
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • v.38 no.4
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    • pp.240-244
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    • 2012
  • Myofibroblastic sarcoma is a rare tumor that mostly develops in the soft tissues of the head and neck. Within the oral cavity, a tongue lesion is the most common. A myofibroblastic sarcoma tends to recur locally instead of metastasizing. We encountered a myofibroblastic sarcoma of the mandible of a 9-year-old male and performed mass excision and additional marginal alveolectomy. So far, there is neither recurrence nor metastasis. We report this case because of the uncommon location of this tumor type and its surgical approach compared to other forms of sarcomas.

Radiologic Findings of Uncommon Breast Cancer (드문(Uncommon) 유방암의 방사선학적 소견)

  • Kim, Jae-Woon;An, Jae-Hong;Hwang, Mi-Soo;Lee, Jae-Kyo;Byun, Woo-Mok
    • Journal of Yeungnam Medical Science
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    • v.15 no.1
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    • pp.114-124
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    • 1998
  • We analyzed the mammographic (n=21) findings (location, margin, shape, cluster microcalcifications, size, multiplicity) and ultrasonographic (n=12) findings (shape, border, internal echo, boundary echo, posterior echo, lateral echo, width/depth ratio) to evaluate specific radiologic findings of histopathologically proved uncommon breast cancer. The mammographic findings (n=21) are as follow; 1) single; 16, multiple; 5 2) margin (smooth; 13, irregular; 4, spiculated; 4) 3) shape (round and ovoid; 9, lobulated; 8, irregular; 4) 4) cluster micro calcifications (abscent; 20, present; 1) 5) size (1-3cm; 18, 3-5cm; 2, 5cm> ; 1) 6) location (UOQ; 13, UIQ; 4, LIQ; 3, LOQ; 1). The ultrasonographic findings (n=12) are as follow; 1) shape (round to oval; 5, lobulated; 5, irregular; 2) 2) border (smooth even; 9, rough uneven; 3) 3) internal echo (fine homogeneous; 5, coarse heterogeneous; 7) 4) boundary echo (regular fine; 4, irregular thick; 8) 5) posterior echo (enhanced; 11, no change; 1) 6) lateral echo (marked; 7, nonexistent; 5) 7) width/depth ratio (1.5> ; 1, 1.0-1.5; 7, 1.0< ; 4). Uncommon breast cancer show benign nature on mammogram, but malignant nature on ultrasonogram (especially boundary echo, internal echo, width/depth ratio).

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An Intramedullary Neurenteric Cyst in the Conus Medullaris with Recurrent Meningitis

  • Park, Yeul-Bum;Kim, Seong-Ho;Kim, Sang-Woo;Chang, Chul-Hoon
    • Journal of Korean Neurosurgical Society
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    • v.41 no.2
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    • pp.130-133
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    • 2007
  • Neurenteric cysts are rare congenital lesions of the spine that are lined with endodermal epithelium. Their most common location is the cervico-dorsal region, and the mass usually lies ventral to the spinal cord. However the conus medullaris area location is an uncommon location. Neurenteric cysts are best treated by decompression and as near total excision of cyst membrane as possible. We report a case of a 7 year-old-girl with a neurenteric cyst in the conus medullaris. The patient had a history of meningitis and a gait disturbance. Magnetic resonance imaging [MRI] showed an intramedullary mass lesion in the conus medullaris with syringomyelia. There was no associated bone or soft-tissue anomaly. The mass was subtotally removed through a posterior approach. However 4 months later, meningeal irritation signs developed and MRI showed recurrence of the cyst. At the second operation, the cystic membrane was totally removed and the patient's neurological symptoms improved postoperatively. We reports a case of recurred neurenteric cyst occurred in unusual location with the review of literature.

On the Distribution of the Movement Speed of Smartphone Users (스마트폰으로 측정된 사용자의 이동속도분포에 관한 연구)

  • Kim, Woojin;Jang, Woncheol;Song, Ha Yoon
    • KIISE Transactions on Computing Practices
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    • v.22 no.11
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    • pp.567-575
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    • 2016
  • With the popularity of smartphone, user's location information is of great interest as mobile apps based on the location information are increasing. In this paper, we are interested in analyzing user's speed data based on the location information. It is not uncommon to observe locations with great measurement errors, removing them is necessary. The distribution of speed can be considered as a mixture model in accordance with transportation means. We identify a tail part as a component of a mixture model and fit a simple parametric model to the tail part of the speed distribution.

Fine Needle Aspiration Cytology of Parapharyngeal Ganglioneuroma - A Case Report - (세침흡인 세포검사로 진단된 인두주위에 발생한 신경절 신경종 - 1예 보고 -)

  • Lee, Ji-Shin;Cho, Hyang-Jeong;Yun, Ki-Jung;Moon, Hyung-Bae
    • The Korean Journal of Cytopathology
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    • v.6 no.2
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    • pp.179-182
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    • 1995
  • Ganglioneuromas are a fully differentiated tumor that contains no immature elements. The majority of sanglioneuromas are diagnosed in patients older than 10 years and are most often located in the posterior mediastinum, followed by the retroperitoneum. The location of these tumors in the parapharyngeal region is extremely uncommon and there are only a few reports on the cytologic appearance of the tumor. We report a case of ganglioneuroma presenting in a parapharyngeal location in a 4 year-old boy, diagnosed by fine needle aspiration cytology. The smears revealed scattered large oval to polygonal cells with voluminous, granular cytoplasms. The nuclei were one to two in number and had a prominent nucleolus. Clusters of benign spindle-shaped cells were also present.

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A Successful Evacuation of Vertex Epidural Hematoma; A Case Report

  • Kim, Jang Hun;Roh, Haewon;Kim, Jong-Hyun;Kwon, Taek-Hyun
    • Journal of Trauma and Injury
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    • v.30 no.3
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    • pp.98-102
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    • 2017
  • Vertex epidural hematoma (VEH) is an uncommon presentation of all epidural hematomas and presents with a wide range of symptom and signs. Diagnosis as well as treatment of VEH is also difficult because of its location adjacent to superior sagittal sinus (SSS). A 43-year-old male visited our hospital after fall down and was diagnosed with VEH. While evaluating its location and patency of SSS, he was deteriorated and urgently underwent evacuation of VEH. Bilateral craniotomies on each side, leaving a central bony island to avoid bleeding of midline structure and provide an anchor for dural tack-ups. After the operation, VEH was totally removed and the patient has restored.

A Case of Granular Cell Tumor of the Vocal Cord (성대의 과립세포종 1례)

  • Jin, Sung-Min;Lee, Jong-Kyu;Kwon, Hee-Jun;Choi, Hyun-Jin
    • Journal of the Korean Society of Laryngology, Phoniatrics and Logopedics
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    • v.17 no.1
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    • pp.60-62
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    • 2006
  • Granular cell tumor is an uncommon lesion that was first described by Abrikossoff in 1926. It is usually benign tumor that can occur in any parts of the body. The most common region of granular cell tumor is the head and neck, accounting for approximately 30 to 50 percent of all lesions, with the tongue as the single most common site of origin. The larynx is uncommon location, accounting for approximately 3 to 10 percent of the reported case. Herein we report a case of a 41-year-old man with laryngeal granular cell tumor who was successfully treated, especially showing well improvements in his voice after the operation. In addition, a brief discussion of the current literatures regarding the typical features of the tumor are also presented.

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A Case of Granular Cell Tumor in the Area of Arytenoid Cartilage (피열연골 부위에 발생한 과립세포종 1례)

  • Sun Dong-Il;Hwang Sung-Jae;Kim Hong-Rae;Kim Min-Sik
    • Korean Journal of Bronchoesophagology
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    • v.11 no.1
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    • pp.28-31
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    • 2005
  • Granular cell tumors are relatively uncommon benign laryngeal lesions thought to originate form Schwann cells. The granular cell tumor occurs everywhere in the body, especially in the head and neck. The larynx is relatively an uncommon location, accounting for approximately 3 to $10\%$ of all reported cases. Typically the most common presenting symptom is hoarseness, with some patients also presenting stridor, hemoptysis, dysphagia, and otlagia. But the tumor may be asymptomatic and discovered only incidentally during a routine examination. The diagnosis of granular cell honor can be confirmed by histopathologically and immunocytochemical staining fer S-100 antigen. Treatment of a granular cell tumor consists of a wide local excision by the endoscopic, transoral or laryngofissure methods. Recently, CO2 laser has been used to remove granular cell tumor with clear resection margin. This article describes one such case in a 62-year-old man, followed by a brief review of the literature on this subject.

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Management of Carotid Body Paraganglioma: Review of the literature with report of three cases (경동맥체 부신경절종)

  • Park Cheong-Soo;Kim Jun-Sik;Hong Won-Pyo;Choi Eun-Chang;Kim Dong-Ik
    • Korean Journal of Head & Neck Oncology
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    • v.5 no.1
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    • pp.5-13
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    • 1989
  • Carotid body paraganglioma is uncommon, with appoximately 900 reports of it in the world literature, and with only 7 documented cases in the Korean literature. The classic carotid body paraganglioma develops in the bifurcation of common carotid artery and involves both the internal and external carotid arteries at it expands. The diagnosis may almost always be established preoperatively by selective angiography which shows a widening of the carotid bifurcation with a well defined vascular mass. Differential consideration of a single, lateral cervical mass in this location include branchial cleft cyst, neurogenic tumor, metastatic thyroid cancer, carotid body aneurysm and salivary gland tumor. Surgical therapy is the preferred method of treatment as these tumors are regarded as radioresistant. Because of their high vascularity and anatomical location, surgical removal of these tumors reguires a considerable degree of caution and a high degree of surgical expertise. With improved diagnostic and surgical technique, the morbidity and mortality has been reduced lately. This report details the management of 3 patients with carotid body paraganglioma who underwent safe resection by subadventitial dissection or using an internal vascular shunt.

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