Literature DB >> 21297584

IgG4 plasma cells in inflammatory myofibroblastic tumor: inflammatory marker or pathogenic link?

Shahrazadb T Saab1, Jason L Hornick, Christopher D Fletcher, Sandra J Olson, Cheryl M Coffin.   

Abstract

Inflammatory myofibroblastic tumor is a rare mesenchymal neoplasm that harbors an anaplastic lymphoma kinase (ALK) gene rearrangement in the majority of cases. It is composed of fibroblastic-myofibroblastic cells with a characteristic inflammatory infiltrate that consists predominantly of plasma cells. In contrast, IgG4-related sclerosing disease is a recently described multisystem disorder with a histological appearance similar to inflammatory myofibroblastic tumor. The plasma cell infiltrate is characteristic in IgG4-related sclerosing disease and has been studied as a tool to render this diagnosis. Histologically, the two disorders overlap, although there are significant clinical differences. This study analyzes the histological appearance of 36 inflammatory myofibroblastic tumors, compares them with IgG4-related sclerosing disease, and assesses the plasma cell profile using immunohistochemistry to determine the range and proportion of IgG4 plasma cells. The majority of patients were children and young adults, mainly with solitary masses and no clinical manifestations of IgG4-related sclerosing disease. ALK-1 positivity was present in 23 cases (64%). None showed obliterative phlebitis or prominent lymphoid aggregates. Of 36 inflammatory myofibroblastic tumors, 15 cases showed an IgG4/IgG ratio ≥0.10, a cutoff described in the literature as supportive of IgG4-related sclerosing disease and up to 33 IgG4-positive plasma cells per high-power field indicating a mild-to-moderate increase as compared with IgG4-related sclerosing disease. Currently, the diagnostic recognition of inflammatory myofibroblastic tumor is based on clinicopathological features and diagnostic adjuncts, such as ALK-1 reactivity and genetic tests. Although inflammatory myofibroblastic tumor and IgG4-related sclerosing disease are distinct entities, a subset of inflammatory myofibroblastic tumors exhibit an IgG4/IgG ratio that is within the range for IgG4-related sclerosing disease. Therefore, the ratio alone cannot be used as a reliable discriminator between these two entities and other clinical and pathologic features must always be taken into account.

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Year:  2011        PMID: 21297584     DOI: 10.1038/modpathol.2010.226

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  28 in total

1.  Etiology analysis and computed tomography imaging of a tonsillar inflammatory myofibroblastic tumor: report of an immunocompetent patient and brief review.

Authors:  Yun-Zhen Luo; Li-Bo Dai; Shui-Hong Zhou; Xing-Mei Luo; Jun Fan; Ling-Xiang Ruan
Journal:  Head Neck Oncol       Date:  2012-03-09

2.  Molecular characterization of inflammatory myofibroblastic tumors with frequent ALK and ROS1 gene fusions and rare novel RET rearrangement.

Authors:  Cristina R Antonescu; Albert J H Suurmeijer; Lei Zhang; Yun-Shao Sung; Achim A Jungbluth; William D Travis; Hikmat Al-Ahmadie; Christopher D M Fletcher; Rita Alaggio
Journal:  Am J Surg Pathol       Date:  2015-07       Impact factor: 6.394

Review 3.  Inflammatory myofibroblastic tumors of the head and nec.

Authors:  Jiang Tao; Min-Li Zhou; Shui-Hong Zhou
Journal:  Int J Clin Exp Med       Date:  2015-02-15

4.  Plasma cell granuloma of the oral cavity: a mucosal manifestation of immunoglobulin G4-related disease or a mimic?

Authors:  Jan Laco; Kateřina Kamarádová; Radovan Mottl; Alena Mottlová; Helena Doležalová; Luboš Tuček; Kamila Žatečková; Radovan Slezák; Aleš Ryška
Journal:  Virchows Arch       Date:  2014-12-19       Impact factor: 4.064

5.  Paraplegia in a Patient With IgG4-Related Sclerosing Disease: A Case Report.

Authors:  Sung Heon Kim; Yeon Kang; Sung Han Oh; Soya Paik; Joo Sup Kim
Journal:  Ann Rehabil Med       Date:  2014-12-24

6.  Pulmonary inflammatory myofibroblastic tumor versus IgG4-related inflammatory pseudotumor: differential diagnosis based on a case series.

Authors:  Longfei Zhu; Jian Li; Chengwu Liu; Wenshuang Ding; Feng Lin; Chenglin Guo; Lunxu Liu
Journal:  J Thorac Dis       Date:  2017-03       Impact factor: 2.895

7.  Idiopathic vs. secondary retroperitoneal fibrosis: a clinicopathological study of 12 cases, with emphasis to possible relationship to IgG4-related disease.

Authors:  Jan Laco; Miroslav Podhola; Kateřina Kamarádová; Ivo Novák; Daniel Dobeš; Miloš Broďák; Mária Hácová; Aleš Ryška
Journal:  Virchows Arch       Date:  2013-09-20       Impact factor: 4.064

8.  An immunoglobulin G4-related sclerosing disease of the small bowel: CT and small bowel series findings.

Authors:  Younghwan Ko; Ji Young Woo; Jeong Won Kim; Hye Sook Hong; Ik Yang; Yul Lee; Daehyun Hwang; Seon Jeong Min
Journal:  Korean J Radiol       Date:  2013-08-30       Impact factor: 3.500

9.  Morphologic Overlap Between Inflammatory Myofibroblastic Tumor and IgG4-related Disease: Lessons From Next-generation Sequencing.

Authors:  Martin S Taylor; Abhijit Chougule; Allsion R MacLeay; Pawel Kurzawa; Ivan Chebib; Long Le; Vikram Deshpande
Journal:  Am J Surg Pathol       Date:  2019-03       Impact factor: 6.394

10.  Inflammatory Myofibroblastic Tumour of Thyroid with its Prominent Spindle Cell Pattern: A Rare Case Report.

Authors:  S Marylilly; T Subachitra; V Ramya
Journal:  J Clin Diagn Res       Date:  2016-04-01
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