Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2010 Feb;22(1):91-5.
doi: 10.5021/ad.2010.22.1.91. Epub 2010 Feb 28.

A case of cutaneous inflammatory myofibroblastic tumor

Affiliations
Case Reports

A case of cutaneous inflammatory myofibroblastic tumor

Soo Bin Son et al. Ann Dermatol. 2010 Feb.

Abstract

Pseudo-inflammatory tumors are also known as plasma cell granuloma, inflammatory pseudo-tumor and inflammatory myofibroblastic tumor, and these tumors are a group of highly variable proliferations of myofibroblastic cells that are associated with a prominent inflammatory infiltrate. This tumor is known to most commonly occur in the lungs, bladder and gastrointestinal system with only a few cases having been reported in the skin. A previously healthy 26-year-old man presented with a 6-year history of an intermittently pruritic lesion on his back. On the histologic examination, there were spindle cells in fascicles and a mixed inflammatory cellular infiltrate of plasma cells and lymphocytes. A diagnosis of inflammatory fibroblastic tumor was made and the nodule was surgically removed. We report here on an additional case of this rare cutaneous entity, and it is probably the first such report from Korea.

Keywords: Myofibroblastic; Pseudo-inflammatory.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
A brownish colored palpable indurated nodule with a rough surface on the upper back.
Fig. 2
Fig. 2
The tumor cells had plump spindle-shaped cytoplasm and the cells were arranged in fascicles or epithelioid nests with collagenous stroma (A: H&E, ×40, B: H&E, ×100). The inflammatory part showed a cellular infiltration that consisted of plasma cells and lymphocytes (C: H&E, ×100, D: H&E, ×200).
Fig. 3
Fig. 3
(A) Staining for smooth muscle actin (SMA) highlights the spindle cells and confirms their myofibroblastic nature (Immunohistochemistry for SMA, ×100). (B) The tumor cells show a weak positive immunoreaction for desmin (Immunohistochemistry for desmin, ×100).

References

    1. Umiker WO, Iverson L. Postinflammatory tumors of the lung; report of four cases simulating xanthoma, fibroma, or plasma cell tumor. J Thorac Surg. 1954;28:55–63. - PubMed
    1. Meis JM, Enzinger FM. Inflammatory fibrosarcoma of the mesentery and retroperitoneum. A tumor closely simulating inflammatory pseudotumor. Am J Surg Pathol. 1991;15:1146–1156. - PubMed
    1. Coffin CM, Watterson J, Priest JR, Dehner LP. Extrapulmonary inflammatory myofibroblastic tumor (inflammatory pseudotumor). A clinicopathologic and immunohistochemical study of 84 cases. Am J Surg Pathol. 1995;19:859–872. - PubMed
    1. Wenig BM, Devaney K, Bisceglia M. Inflammatory myofibroblastic tumor of the larynx. A clinicopathologic study of eight cases simulating a malignant spindle cell neoplasm. Cancer. 1995;76:2217–2229. - PubMed
    1. Sciot R, Dal Cin P, Fletcher CD, Hernandez JM, Garcia JL, Samson I, et al. Inflammatory myofibroblastic tumor of bone: report of two cases with evidence of clonal chromosomal changes. Am J Surg Pathol. 1997;21:1166–1172. - PubMed

Publication types

LinkOut - more resources