Loading [MathJax]/jax/output/HTML-CSS/fonts/TeX/fontdata.js

Journal List > Arch Hand Microsurg > v.22(4) > 1106609

Ahn, Choi, and Lee: Metachronous Sarcoma: A Case of Pleomorphic Leiomyosarcoma in a Patient with a History of Fibrosarcoma

초록

Metachronous cancers were defined as those that were detected after an interval of more than 6 months. The instance of two histologically distinct sarcomas in one patient is very unusual. A 42-year-old woman presented for evaluation of a painless mass in her right axilla area. She gave a history of operation 8 years ago for treating a fibrosarcoma on her right upper arm at local clinic. Eight years ago, the lesion was widely excised. Magnetic resonance imaging revealed a new generated tumor at her right axilla. After a wide surgical resection, we performed anterolateral thigh free flap for cover the defect. Second neoplasm is leiomyosarcoma. These two neoplasms are 2 histologically distinct tumors. There is no report of a case of metachronous soft tissue sarcoma both pleomorphic leiomyosarcoma and fibrosarcoma in upper extremity within one person. We emphasize the importance of considering the possibility of metachronous sarcoma.

Go to : Goto

REFERENCES

1.Daigeler A., Lehnhardt M., Sebastian A, et al. Metachronous bilateral soft tissue sarcoma of the extremities. Lan-genbecks Arch Surg. 2008. 393:207–12.
crossref
2.Tukiainen E., Böhling T., Huuhtanen R. Soft tissue sarcoma of the trunk and extremities. Scand J Surg. 2003. 92:257–63.
crossref
3.Pitcher ME., Fish S., Thomas JM. Management of soft tissue sarcoma. Br J Surg. 1994. 81:1136–9.
crossref
4.Dei Tos AP. Classification of pleomorphic sarcomas: where are we now? Histopathology. 2006. 48:51–62.
5.Folpe AL. Fibrosarcoma: a review and update. Histopathology. 2014. 64:12–25.
crossref
6.Warren S., Gates O. Multiple primary malignant tumors. A survey of the literature and statistical study. Am J Cancer. 1932. 16:1358–414.
7.Grobmyer SR., Luther N., Antonescu CR., Singer S., Bren-nan MF. Multiple primary soft tissue sarcomas. Cancer. 2004. 101:2633–5.
crossref
8.Picardo NE., Mann B., Whittingham-Jones P., Shaerf D., Skinner JA., Saifuddin A. Bilateral symmetrical metachronous myxofibrosarcoma: a case report and review of the literature. Skeletal Radiol. 2011. 40:1085–8.
crossref
9.Grimer R., Judson I., Peake D., Seddon B. Guidelines for the management of soft tissue sarcomas. Sarcoma. 2010. 2010:506182.
crossref
Go to : Goto

ahm-22-299f1.tif
Fig.1.
Microscopic examinations of the fibrosarcoma. The mass is composed of short spindle cell fascicles arranged haphazardly with some eosinophilic collagen fiber (H&E, ×200).
undefined
ahm-22-299f2.tif
Fig.2.
A magnetic resonance imaging revealed a new generated tumor at her right axilla.
undefined
ahm-22-299f3.tif
Fig.3.
Gross examination of the pleomorphic leiomyosarcoma. The mass is a well-demarcated nodular, and located between subcutaneous fat tissue and skeletal muscular tissue. The cut surface reveals homogeneous grey whitish solid nature.
undefined
ahm-22-299f4.tif
Fig.4.
Microscopic examinations of the pleomorphic leiomyosarcoma. The mass is composed of marked pleomorphic short spindle cells arranged haphazardly (H&E, ×400).
undefined
ahm-22-299f5.tif
Fig.5.
Excision site with free flap coverage was healed well and there was only little scar. There was no evidence of re-currence and metastasis.
undefined
TOOLS
Similar articles