Mesenteric Tumor of an Infant: A Clinical and Pathological Surprise

Authors

  • Md Ali Osama Department of Pathology, Lady Hardinge Medical College, New Delhi https://orcid.org/0000-0002-0660-9939
  • Smita Singh Department of Pathology, Lady Hardinge Medical College, New Delhi
  • Sahaj Prajapati Department of Paediatric Surgery, Lady Hardinge Medical College, New Delhi
  • Subhasis Roy Choudhury Department of Paediatric Surgery, Lady Hardinge Medical College, New Delhi
  • Nishat Amina Department of Radiology, Lady Hardinge Medical College, New Delhi

DOI:

https://doi.org/10.21276/apalm.3143

Keywords:

Anaplastic lymphoma kinase-1, colon, inflammatory myofibroblastic tumor, mesentery

Abstract

Inflammatory myofibroblastic tumor (IMT) is a tumefactive proliferation of spindled myofibroblastic cells admixed with inflammatory infiltrate. This tumor has a predilection for pulmonary location and also involves visceral soft tissues in children and adults. Tumors in extrapulmonary locations like abdomen, mesentery, bowel, head & neck, genitourinary and musculoskeletal are more aggressive locally and mimic malignancy. IMTs from colon are very rare and are treated by surgical excision. We report a case of a 9-month old female with IMT of sigmoid colon with no bowel complaints, treated by complete surgical excision with no further treatment needed.

References

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Published

02-02-2022

How to Cite

1.
Osama MA, Singh S, Prajapati S, Choudhury SR, Amina N. Mesenteric Tumor of an Infant: A Clinical and Pathological Surprise. Ann of Pathol and Lab Med [Internet]. 2022 Feb. 2 [cited 2024 Nov. 19];9(1):C4-7. Available from: https://pacificejournals.com/journal/index.php/apalm/article/view/3143

Issue

Section

Case Report