Introduction. Hodgkin Lymphoma (HL) is one of the most curable malignant diseases. Modern treatments, like the combined radiochemotherapy and stem cell transplantation, have increased the number of malignant disease survivors. However, HL survivors are at risk of long-term effects, including the development of solid tumors. Secondary neoplasms are a major cause of late morbidity and mortality following treatment for HL. Case report. We report the case of a male patient, treated for HL by chemotherapy, who developed a large leiomyoma of the cecum one year after the treatment. A whole-body Magnetic Resonance (WBMRI) scan performed during the follow-up allowed the detection of this incidental caecal mass that was absent in a Computed Tomography (CT) scan performed immediately after the treatment. After a CT-guided biopsy, the lesion was surgically removed and the diagnosis of caecal leiomyoma was obtained. Discussion. To our knowledge, this is the first case report, according to the scientific literature, of caecal leiomyoma developing after chemotherapy in a HL survivor. Leiomyoma is a rare benign tumor that usually appears as a solitary small mass with a nodular growth and a benign course. Conclusion. This case shows that WB-MRI allows detecting relevant incidental findings during the oncologic follow-up, avoiding both radiation exposure and contrast agent administration. Furthermore, leiomyoma should be considered in the differential diagnosis between the caecal masses with high growth rate.

Albano, D., Sinagra, E., Patti, C., Narese, D., Agrusa, A., Di Buono, G., et al. (2017). Caecal leiomyoma detected by whole-body MRI in a patient with hodgkin lymphoma: First case report. IL GIORNALE DI CHIRURGIA, 38(1), 27-32 [10.11138/gchir/2017.38.1.027].

Caecal leiomyoma detected by whole-body MRI in a patient with hodgkin lymphoma: First case report

ALBANO, Domenico;SINAGRA, Emanuele;PATTI, CARLO;NARESE, Donatella;AGRUSA, Antonino;DI BUONO, Giuseppe;MIDIRI, Massimo;LAGALLA, Roberto;GALIA, Massimo
2017-01-01

Abstract

Introduction. Hodgkin Lymphoma (HL) is one of the most curable malignant diseases. Modern treatments, like the combined radiochemotherapy and stem cell transplantation, have increased the number of malignant disease survivors. However, HL survivors are at risk of long-term effects, including the development of solid tumors. Secondary neoplasms are a major cause of late morbidity and mortality following treatment for HL. Case report. We report the case of a male patient, treated for HL by chemotherapy, who developed a large leiomyoma of the cecum one year after the treatment. A whole-body Magnetic Resonance (WBMRI) scan performed during the follow-up allowed the detection of this incidental caecal mass that was absent in a Computed Tomography (CT) scan performed immediately after the treatment. After a CT-guided biopsy, the lesion was surgically removed and the diagnosis of caecal leiomyoma was obtained. Discussion. To our knowledge, this is the first case report, according to the scientific literature, of caecal leiomyoma developing after chemotherapy in a HL survivor. Leiomyoma is a rare benign tumor that usually appears as a solitary small mass with a nodular growth and a benign course. Conclusion. This case shows that WB-MRI allows detecting relevant incidental findings during the oncologic follow-up, avoiding both radiation exposure and contrast agent administration. Furthermore, leiomyoma should be considered in the differential diagnosis between the caecal masses with high growth rate.
2017
Settore MED/18 - Chirurgia Generale
Settore MED/36 - Diagnostica Per Immagini E Radioterapia
Albano, D., Sinagra, E., Patti, C., Narese, D., Agrusa, A., Di Buono, G., et al. (2017). Caecal leiomyoma detected by whole-body MRI in a patient with hodgkin lymphoma: First case report. IL GIORNALE DI CHIRURGIA, 38(1), 27-32 [10.11138/gchir/2017.38.1.027].
File in questo prodotto:
File Dimensione Formato  
Caecal leiomyoma.pdf

accesso aperto

Descrizione: full text
Dimensione 963.64 kB
Formato Adobe PDF
963.64 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/239752
Citazioni
  • ???jsp.display-item.citation.pmc??? 1
  • Scopus 2
  • ???jsp.display-item.citation.isi??? 1
social impact