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Case Reports
. 2022 Mar 18;14(3):e23289.
doi: 10.7759/cureus.23289. eCollection 2022 Mar.

Anaplastic Lymphoma Kinase (ALK)-Negative Inflammatory Myofibroblastic Tumor of the Kidney in a Nine-Month-Old Girl

Affiliations
Case Reports

Anaplastic Lymphoma Kinase (ALK)-Negative Inflammatory Myofibroblastic Tumor of the Kidney in a Nine-Month-Old Girl

Bisma Tareen et al. Cureus. .

Abstract

An inflammatory myofibroblastic tumor (IMT) is an uncommon, benign tumor of myofibroblastic spindle cells. An IMT can occur in any part of the body. However, involving kidney is exceedingly rare. When this rare entity occurs in children, it becomes incredibly challenging to distinguish this rare entity from other malignancies such as Wilms tumor. Although imaging studies of the abdomen and pelvis add to the diagnosis, however, histological examination and immunohistochemical staining remain the gold standard for the precise diagnosis of this rare entity. To the best of our knowledge, only 48 cases of renal IMT have been published in the medical literature so far. We report the case of a nine-month-old girl who was brought with complaints of hematuria, and later, imaging and histological confirmation revealed an anaplastic lymphoma kinase (ALK)-negative IMT of the kidney.

Keywords: benign; ct (computed tomography) imaging; hematuria; inflammatory myofibroblastic tumor; wilms tumor.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. MRI revealing well-defined, predominantly solid hypoenhancing right renal mass with a small cystic area in the periphery of the lesion
Figure 2
Figure 2. Gross examination: well-circumscribed lesion with focal hemorrhage
Figure 3
Figure 3. Histological examination: hematoxylin and eosin stain (H&E)
A, B, H&E and bland spindle cells with mixed inflammatory infiltrate. C, Spindle cells showed nuclear and cytoplasmic positivity for cyclin D1. D, Spindle cells are negative for ALK stain. ALK: anaplastic lymphoma kinase.

References

    1. Inflammatory myofibroblastic tumor of the kidney in a child: report of a case. Boo YJ, Kim J, Kim JH, Kim CS, Suh SO. Surg Today. 2006;36:710–713. - PubMed
    1. A case of renal inflammatory pseudotumor leading to nephrectomy. Tuan Linh L, Minh Duc N, Tra My TT, Nhan Hien P, Ngoc Minh T, Van Lenh B. J Investig Med High Impact Case Rep. 2021;9:23247096211003224. - PMC - PubMed
    1. Unusual presentation of lipofibromatosis-like neural tumor in an adult: a case report. Zarak MS, Sliker T, Javadi T, et al. Saudi J Med Med Sci. 2021;9:267–270. - PMC - PubMed
    1. Inflammatory myofibroblastic tumor of the kidney and bilateral lung nodules in a child mimicking Wilms tumor with lung metastases. Dogan MS, Doganay S, Koc G, Gorkem SB, Unal E, Ozturk F, Coskun A. J Pediatr Hematol Oncol. 2015;37:0–3. - PubMed
    1. Inflammatory myofibroblastic tumor associated with renal cell carcinoma. Gwynn ES, Clark PE. Urology. 2005;66:880–889. - PubMed

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