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Nadir Görülen Bir Akciğer Tümörü: İnflamatuvar Myofibroblastik Tümör

Year 2022, Volume: 17 Issue: 1, 208 - 211, 21.03.2022
https://doi.org/10.17517/ksutfd.869381

Abstract

İnflamatuar myofibroblastiktümör (IMT), nadir görülen bir yumuşak doku tümörüdür. Çoğunlukla benign karakterli olmakla birlikte biyolojik davranışı tartışmalıdır.
Öksürük şikayeti ile polikliniğimize başvuran kadın hastayı radyolojik ve histopatoloijk olarak değerlendirdik. Sağ akciğer alt lobda tespit ettiğimiz mass lezyonun histopatolojik tanısı inflamatuar myofibroblastik tümör olarak raporlandı. Radyolojik olarak malign tümörlerden ayırt edilmeyen bu nadir olguyu literatür bilgileri eşliğinde sunmayı amaçladık.
IMT’nin radyolojik bugularla malign tümörlerden ayırt edilmesi güçtür. Total rezeksiyonla hem tanı hem de tedavisi mümkündür.

References

  • 1. Furkan Ufuk, Duygu Herek, Nevzat Karabulut Inflammatory Myofibroblastic Tumor of the Lung: Unusual Imaging Findings of Three Cases-Pol J Radiol. 2015; 80: 479–482
  • 2. Ekinci GH, Haciomeroglu O, Sen AC, Alpay L, Guney PA, Yilmaz A.J Coll Physicians Surg Pak. 2016 Apr;26(4):331-3.
  • 3. Ozkan Demirhan, Selvinaz Ozkara, Mustafa Yaman, Kamil Kaynak Respir Med Case Rep. 2013; 8: 32–35.
  • 4. Matsubara O, Tan-Liu NS, Kenney RM, Mark EJ. Inflammatory pseudotumors of the lung: progression from organizing pneumonia to fibrous histiocytoma or to plasma cell granuloma in 32 cases. Hum Pathol. 1988;19(7):807–14.
  • 5. Lee HJ, Kim JS, Choi YS, Kim K, Shim YM, Han J, et al. Treatment of inflammatory myofibroblastic tumor of the chest: The extent of resection. Annals of Thoracic Surgery. 2007;84:221–224

A Rarely Seen Lung Tumor: Inflammatory Myofibroblastic Tumor

Year 2022, Volume: 17 Issue: 1, 208 - 211, 21.03.2022
https://doi.org/10.17517/ksutfd.869381

Abstract

Inflammatory myofibroblastic tumor (IMT) is a rarely seen soft tissue tumor. Although it is mostly benign, its biological behaviour is controversial.
We radiologically and histopathologically evalauted a female patient admitted to our outpatient clinic due to complaint of cough. Histopathologic diagnosis of mass lesion identified at lower lobe of right lung was reported as inflammatory myofibroblastic tumor. We aimed to present this rare case which is not radiologically differentiable from malignant tumors along with literature data.
Differentiating IMT from malignant tumor with radiologic findings is difficult. Both treatment and the diagnosis are possible with total resection.

References

  • 1. Furkan Ufuk, Duygu Herek, Nevzat Karabulut Inflammatory Myofibroblastic Tumor of the Lung: Unusual Imaging Findings of Three Cases-Pol J Radiol. 2015; 80: 479–482
  • 2. Ekinci GH, Haciomeroglu O, Sen AC, Alpay L, Guney PA, Yilmaz A.J Coll Physicians Surg Pak. 2016 Apr;26(4):331-3.
  • 3. Ozkan Demirhan, Selvinaz Ozkara, Mustafa Yaman, Kamil Kaynak Respir Med Case Rep. 2013; 8: 32–35.
  • 4. Matsubara O, Tan-Liu NS, Kenney RM, Mark EJ. Inflammatory pseudotumors of the lung: progression from organizing pneumonia to fibrous histiocytoma or to plasma cell granuloma in 32 cases. Hum Pathol. 1988;19(7):807–14.
  • 5. Lee HJ, Kim JS, Choi YS, Kim K, Shim YM, Han J, et al. Treatment of inflammatory myofibroblastic tumor of the chest: The extent of resection. Annals of Thoracic Surgery. 2007;84:221–224
There are 5 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Olgu Sunumları
Authors

Fatoş Kozanlı 0000-0001-7664-2657

Abdulkadir Yasir Bahar 0000-0002-6963-3389

Publication Date March 21, 2022
Submission Date January 29, 2021
Acceptance Date April 18, 2021
Published in Issue Year 2022 Volume: 17 Issue: 1

Cite

AMA Kozanlı F, Bahar AY. A Rarely Seen Lung Tumor: Inflammatory Myofibroblastic Tumor. KSU Medical Journal. March 2022;17(1):208-211. doi:10.17517/ksutfd.869381