Literature DB >> 10705720

Pulmonary hamartoma. A rare case report.

L Panzini1, S Potalivo, G Saed, M Rapisarda, A Bisetti.   

Abstract

Pulmonary hamartoma is a rare lung neoformation, usually symptomless and by chance discovered, of a probable dysontogenetic origin with prevailing cartilaginous tissue and adult, onset age. The Authors report a rare case of a 25-year-old student, symptomless and fortuitously found by means of a radiograph of the chest. Many interesting features characterize the case report: histological nature of the pulmonary hamartoma, mainly vascular, so much as to feign an angiosarcoma at the macroscopical examination, and with small peripheral calcifications as shown by lung CT scan; the measures (about 7 cm) plentifully above the parameters usually reported in the literature (from 2 cm to 4 cm); the young onset age (about 10 years old). We may consider a case exceptionally reported in the literature. Besides, on the base of a few studies and of our experience, the results of the pulmonary hamartoma growth rate and doubling time are reported.

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Year:  1999        PMID: 10705720

Source DB:  PubMed          Journal:  Panminerva Med        ISSN: 0031-0808            Impact factor:   5.197


  1 in total

1.  Primary Pulmonary Sequestration With Secondary Hamartomatosis Change.

Authors:  Changhu Liang; Shifeng Xu; Bin Zhao; Guoyuan Ma; Yinglin Du
Journal:  Iran J Radiol       Date:  2015-07-22       Impact factor: 0.212

  1 in total

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