Multifocal sclerosing angiomatoid nodular transformation of the spleen: a case report and review of literature
Autor: | Qiang-Xiu Wang, Jiawen Xu, Jia-Mei Li, Zhi-xin Cao, Jian-Feng Li |
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Rok vydání: | 2015 |
Předmět: |
Adult
Male Pathology medicine.medical_specialty Histology Biopsy Treatment outcome Case Report Spleen Laparoscopic splenectomy Sclerosing angiomatoid nodular transformation Pathology and Forensic Medicine X ray computed medicine Humans IgG4-related sclerosing disease Splenic Diseases Histiocytoma Benign Fibrous business.industry Multiple nodules Nodule (medicine) General Medicine medicine.disease Immunohistochemistry Treatment Outcome Tomography x ray computed medicine.anatomical_structure Male patient Splenectomy Laparoscopy Splenic disease medicine.symptom Tomography X-Ray Computed business Biomarkers |
Zdroj: | Diagnostic Pathology |
ISSN: | 1746-1596 |
DOI: | 10.1186/s13000-015-0312-2 |
Popis: | Sclerosing angiomatoid nodular transformation (SANT) is a relatively new entity in the spleen, which usually presents in the form of single nodule. Only 5 multifocal SANT cases have been reported in English literature. The present case is the first report of a 38-years-old male patient with SANT in the form of multiple nodules, who has been cured via laparoscope. In comparison to solitary SANT, multifocal SANT occurs more likely in males than females and association with malignant neoplasm has not been described yet. Multifocal SANT as well as solitary SANT show some relationships with IgG4-related sclerosing disease. Electronic supplementary material The online version of this article (doi:10.1186/s13000-015-0312-2) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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