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Angiomatous Nasal Polyp with Maxillary Wall Erosion

Kim JY, Nam SY, Kwon SJ, Jun SY

  • KMID: 2297672
  • J Rhinol.
  • 2007 Nov;14(2):125-127.
An angiomatous polyp originates from a sinochoanal polyp, and may be confused with a vascular neoplasm. Compromise of their vascular supply may occasionally lead to infarction, resulting in clinical, radiological...
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Three Cases of Arteriovenous Hemangioma

Kim MJ, Shin N, Cho S, Whang KK, Hahm JH

  • KMID: 2303280
  • Korean J Dermatol.
  • 2000 Apr;38(4):506-511.
We experienced three cases of arteriovenous hemangioma in middle-aged patients. Each of them an asymptomatic small red to purple papule on the face and arm, which showed typical microscopic features...
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Osteo-nevus of Nanta

Oh YJ, Lee EJ, Shin MK, Lee MH

  • KMID: 2247699
  • Korean J Dermatol.
  • 2010 Jun;48(6):525-528.
Cutaneous ossification is an unusual event, and it may be primary or secondary to either inflammatory or neoplastic processes. It is classified as primary when it occurs in the absence...
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The Role of Pericranial Flap in Surgery of Craniosynostosis

Byeon JH, Yim YM, Yoo G

  • KMID: 2203465
  • J Korean Soc Plast Reconstr Surg.
  • 2005 Mar;32(2):189-193.
Reconstruction of calvarial bone defects from congenital anomaly or from bone loss due to traumatic or neoplastic processes remains a significant problem in craniofacial surgery and neurosurgery. To facilitate bone...
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Two Cases of Infantile Intra-abdominal Inflammatory Myofibroblastic Tumor

Kim SH, Cho YH, Kim HY

  • KMID: 2315476
  • Pediatr Gastroenterol Hepatol Nutr.
  • 2014 Jun;17(2):116-120.
Inflammatory myofibroblastic tumor (IMT) is rare mesenchymal solid tumor that consists of proliferating myofibroblasts with an inflammatory infiltrate background. It has a very low prevalence in infants and occurs mainly...
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Extragastroesophageal Malignancy-Associated Secondary Achalasia: A Rare Association of Pancreatic Cancer Rendering Alarm Manifestation

Kim HM, Chu JM, Kim WH, Hong SP, Hahm KB, Ko KH

Secondary achalasia or pseudoachalasia is a rare esophageal motor abnormality, which mimics primary achalasia; it is not easily distinguishable from idiopathic achalasia by manometry, radiological examination, or endoscopy. Although the...
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