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ÆóÀÇ Çظé¾ç Ç÷°üÁ¾ -1¿¹ º¸°í- Pulmonary Cavernous Hemangioma - A case report -

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Abstract

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The pulmonary cavernous hemangioma is usually from birth and there may be
without symptoms until adulthood. Larger or multiple pulmonary angiomata with
considerable pulmonary arteriovenous shunts may cause cyanosis, finger clubbing,
dyspnea and frequently accompanying bruit.
Recently, we experienced a case of cavernous hemangioma of the lung.434-year-old
woman was admitted to our hospital for surgical evaluation of a 4 cm solitary, round
nodule in the right upper lobe on the chest X-ray and CT scan. She had no symptoms.
Laboratory findings are with-in normal limits except for elevated glucose levels.
At surgery, the mass was well encapsulated and easily excised from the peripheral
portion of the posterior segment of the right upper lobe. Grossly, it consisted of a 4 §¯
in diameter, round, soft, sponge-like, hemorrhagic, slightly lobulated mass with a smooth
external surface. Microscopically, the mass was composed of vessels, which were thin
walled, dilated and filled with blood. The wall of the abnormal vessels was thin and
composed of endothelium and fibrous connective tissue with only a little smooth muscle.
Immunohistochemically, the wall of the dilated abnormal vessesls showed negative
reaction for cytokeratin(low and high) and epithelial membrane antigen but weakly
positive reaction for UEA-1 in focal areas.

Å°¿öµå

Hemangioma; Cavernous; Pulmonary;

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