Imaging of Primary Chest Wall Tumors with Radiologic-Pathologic Correlation
Author(s) -
Se Jin Nam,
Sung Jun Kim,
Beom Jin Lim,
Choon-Sik Yoon,
Tae Hoon Kim,
JinSuck Suh,
Doo Hoe Ha,
Jong Won Kwon,
Young Cheol Yoon,
Hye Won Chung,
Mi Sook Sung,
Yun Sun Choi,
Jang Gyu
Publication year - 2011
Publication title -
radiographics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.866
H-Index - 172
eISSN - 1527-1323
pISSN - 0271-5333
DOI - 10.1148/rg.313105509
Subject(s) - medicine , differential diagnosis , soft tissue , radiology , pathology , hemosiderin
Neoplasms and tumorlike lesions that originate from chest wall tissues are uncommon compared with tumors in other parts of the body, and unfamiliarity with these disease entities can cause diagnostic difficulties for radiologists. Furthermore, the imaging features of many of these tumors are nonspecific, particularly those that are locally aggressive. However, a systematic approach based on patient age, clinical history, lesion location, and characteristic imaging findings often helps limit the differential diagnosis. Primary chest wall tumors can be classified as bone or soft-tissue tumors, with the latter being further classified into adipocytic tumors, vascular tumors, peripheral nerve sheath tumors, cutaneous lesions, fibroblastic-myofibroblastic tumors, and so-called fibrohistiocytic tumors, largely based on the 2002 World Health Organization classification. Within each category, it is possible to further limit the differential diagnosis with cross-sectional imaging. Information on specific features (eg, mineralization, fibrosis, hemosiderin deposits) and imaging patterns (eg, the "target sign" and "fascicular sign" seen in neurogenic tumors) can aid in making the diagnosis. Radiologists can achieve a sufficiently specific diagnosis of bone tumors and soft-tissue tumors if typical findings are present.
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