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Bradatsch, A; Kornprat, P; Haybaeck, J; Mischinger, HJ.
A case report of an intraabdominal microcystic and pseudopapillary spindle and round cell neoplasm and a comparison to other intraabdominal mesenchymal tumors.
Anticancer Res. 2013; 33(3):991-995 (- Case Report)
Web of Science PubMed

 

Führende Autor*innen der Med Uni Graz
Kornprat Peter
Simon Andrea
Co-Autor*innen der Med Uni Graz
Haybäck Johannes
Mischinger Hans-Jörg
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Abstract:
We present a case of a new mesenchymal tumor entity named 'distinctive microcystic and pseudopapillary spindle and round cell neoplasm', of which only 30 cases have been reported worldwide. A fifty-two-year-old woman presented in January 2012 with epigastric pain of changing character and weight loss. Examinations revealed a tumor 10×6.8×9.8 cm in diameter showing infiltration in the surrounding organs. A Whipple procedure and a right hemicolectomy were necessary to achieve free resection margins. At the last follow-up in November 2012 the patient was well and there were no signs of recurrence or metastatic spread. Intra-abdominal mesenchymal tumors cause unspecific abdominal symptoms. Local recurrence and metastatic spread can occur. The main prognostic factors for survival are a free margin after resection and the histological subtype of the tumor. Behavioral prediction is not possible in every case and the treatment has to be individualized for every patient. This case represents a new entity of mesenchymal tumor. It was treated according to the guidelines for intra-abdominal sarcomas. Further investigation of this kind of tumor is necessary to define therapeutic guidelines.
Find related publications in this database (using NLM MeSH Indexing)
Abdominal Neoplasms - pathology
Female -
Gastrointestinal Stromal Tumors - pathology
Humans -
Mesenchymoma - pathology
Middle Aged -
Sarcoma - pathology
Tomography, X-Ray Computed -

Find related publications in this database (Keywords)
Mesenchymal tumor
GIST
sarcoma
spindle cell
round cell
pseudopapillary
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