The role of "penumbra sign" and diffusion-weighted imaging in adnexal masses: do they provide a clue in differentiating tubo-ovarian abscess from ovarian malignancy?

Ranjan Kumar Patel, Anju Garg, Rashmi Dixit, Gauri Gandhi, Nita Khurana, Ranjan Kumar Patel, Anju Garg, Rashmi Dixit, Gauri Gandhi, Nita Khurana

Abstract

Purpose: To evaluate the role of "penumbra sign", diffusion-weighted imaging (DWI), and the apparent diffusion coefficient (ADC) value in differentiating tubo-ovarian abscess (TOA) from ovarian malignancy.

Material and methods: Thirty-six patients with 50 adnexal masses (tubo-ovarian abscess, n = 24; ovarian malignancy, n = 26), who underwent magnetic resonance imaging (MRI) with DWI, were retrospectively evaluated. "Penumbra sign" (hyperintense rim on T1W images), diffusion restriction, and mean apparent diffusion coefficient (ADC) values from cystic (c-ADC) and solid (s-ADC) components were evaluated for all the masses.

Results: "Penumbra sign" on T1W images was significantly more common in the TOA group (n = 21, 87.5%) than in the ovarian malignancy group (n = 2, 7.7%) (p < 0.001). Similarly, diffusion restriction in the cystic component was more frequent in the TOA group (n = 24, 100% vs. n = 2, 10.5%; p < 0.001). In contrast, diffusion restriction in the solid component was more common in the ovarian malignancy group (n = 5, 20.8% vs. n = 26, 100%; p < 0.001). The mean c-ADC value was significantly lower in TOAs (p < 0.001). A c-ADC value of 1.31 × 10-3 mm2/s may be an optimal cut-off in distinguishing TOAs from ovarian malignancies. Conversely, the mean s-ADC value was significantly lower in the ovarian malignancy group (p < 0.001). An s-ADC value of 0.869 × 10-3 mm2/s may be an optimal cut-off in differentiating ovarian malignancies from TOAs (p < 0.001). ROC curve analysis showed that c-ADC values had a higher diagnostic accuracy than s-ADC values.

Conclusions: "Penumbra sign" on T1W images, diffusion characteristics, and ADC values provide important clues in addition to conventional MR imaging features in differentiating TOA from ovarian malignancy.

Keywords: apparent diffusion coefficient (ADC); conventional MRI; diffusion-weighted imaging (DWI); ovarian malignancy; penumbra sign; tubo-ovarian abscess (TOA).

Conflict of interest statement

The authors report no conflict of interest.

Copyright © Polish Medical Society of Radiology 2021.

Figures

Figure 1
Figure 1
Penumbra sign on T1-weighted images. A) Right tubo-ovarian abscess shows a complex adnexal mass with hyperintense rim along the inner walls of cavities (white arrows) – termed as “penumbra sign”. B) The cavity of tubo-ovarian abscess in another patient also shows hyperintense rim (white arrows)
Figure 2
Figure 2
Left-sided tubo-ovarian abscess in a 21-year-old female. A) Axial T2W image shows a complex solid-cystic right adnexal mass with a few incomplete septae (yellow arrows). B) Axial T1W image shows “penumbra sign” (white arrows B). C) CE-T1W image depicts enhancing thick irregular septae, solid peripheral component, and irregular enhancement in the surrounding. D) DWI image showing marked diffusion restriction in the abscess cavity (red asterisks) with (E) low ADC values (minimum ADC of 0.560 × 10-3 mm2/s); F) solid component appears hypointense on DWI with higher ADC values (minimum value of 1.305 × 10-3 mm2/s)
Figure 3
Figure 3
Right tubo-ovarian abscess (tubercular) in a 32-year-old female. A) Axial T2W image shows a complex solid cystic right adnexal mass of intermediate signal intensity. B) Axial T1W image at a slightly lower level shows “penumbra sign” around the abscess cavity (white arrows). C) Post-contrast T1WI image showing enhancing solid components. D) DWI image shows marked diffusion restriction in cystic areas (red arrows) with a minimum ADC value of 0.352 × 10-3 mm2/s (E), whereas solid tissue (F) does not show diffusion restriction with an ADC value of 1.153 × 10-3 mm2/s
Figure 4
Figure 4
Bilateral ovarian serous cystadenocarcinoma. Axial T2W (A) and T1W (B) images show complex T2 intermediate and T1 hypointense multilocular solid-cystic masses in bilateral adnexae with multiple papillary projections (red arrows A); no “penumbra sign” is noted; contrast-enhanced T1W image (C) shows enhancing solid components and septae. Axial DW image (D) reveals marked diffusion restriction in the solid areas (white arrows) with (E) low ADC values (minimum ADC value of 0.565 × 10-3 mm2/s); F) cystic component showing facilitated diffusion with higher ADC values (minimum value of 2.495 × 10-3 mm2/s)
Figure 5
Figure 5
Juvenile granulosa cell tumour of the left ovary. Axial T2W (A) and T1W Non-FS (B) images show a well-defined T2 intermediate and T1 hypointense solid-cystic left ovarian mass; few T1 hyperintense cystic areas are noted (yellow arrows B), indicating haemorrhage; T1W image (C) at a lower section showing a T1 hyperintense rim around the cyst (white arrow C); post-contrast T1WI image (D) shows enhancing solid component; axial DWI image (E) depicts high signal in the solid as well as cystic (red arrows E and F) areas with low signal on corresponding ADC map (F), suggesting diffusion restriction; ADC value measured in the solid area is 0.837 × 10-3 mm2/s
Figure 6
Figure 6
ROC curves analysis show greater area under the curve (AUC) for c-ADC values (A) than that of s-ADC values (B), indicating that c-ADC has higher diagnostic accuracy than s-ADC in differentiating a tubo-ovarian mass from an ovarian malignancy

References

    1. Landers DV, Sweet RL. Tubo-ovarian abscess: contemporary approach to management. Rev Infect Dis 1983; 5: 876-884.
    1. Lareau SM, Beigi RH. Pelvic inflammatory disease and tubo-ovarian abscess. Infect Dis Clin North Am 2008; 22: 693-708.
    1. But I, Reljic M. The value of serum CA 125 for the management of tubo-ovarian abscesses. Wien Klin Wochenschr 2000; 112: 1044-1048.
    1. Ha HK, Lim GY, Cha ES, et al. . MR imaging of tubo-ovarian abscess. Acta Radiol 1995; 36: 510-514.
    1. Rakheja R, Makis W, Hickeson M. Bilateral tubo-ovarian abscess mimics ovarian cancer on MRI and (18)F-FDG PET/CT. Nucl Med Mol Imaging 2011; 45: 223-228.
    1. Curry A, Williams T, Penny ML. Pelvic inflammatory disease: diagnosis, management, and prevention. Am Fam Physician 2019; 100: 357-364.
    1. Garcia-Eulate R, Hussain N, Heller T, et al. . CT and MRI of hepatic abscess in patients with chronic granulomatous disease. AJR Am J Roentgenol 2006; 187: 482-490.
    1. Grey AC, Davies AM, Mangham DC, Grimer RJ, Ritchie DA. The ‘penumbra sign’ on T1-weighted MR imaging in subacute osteomyelitis: frequency, cause and significance. Clin Radiol 1998; 53: 587-592.
    1. Foti PV, Attinà G, Spadola S, et al. . MR imaging of ovarian masses: classification and differential diagnosis. Insights Imaging 2016; 7: 21-41.
    1. Fan H, Wang TT, Ren G, et al. . Characterization of tubo-ovarian abscess mimicking adnexal masses: Comparison between contrastenhanced CT, 18F-FDG PET/CT and MRI. Taiwan J Obstet Gynecol 2018; 57: 40-46.
    1. Thomassin-Naggara I, Toussaint I, Perrot N, et al. . Characterization of complex adnexal masses: value of adding perfusion-and diffusion-weighted MR imaging to conventional MR imaging. Radiology 2011; 258: 793-803.
    1. Ebisu T, Tanaka C, Umeda M, et al. . Discrimination of brain abscess from necrotic or cystic tumors by diffusion-weighted echo planar imaging. Magn Reson Imaging 1996; 14: 1113-1116.
    1. Kim HJ, Lee SY, Shin YR, Park CS, Kim K. The value of diffusion-weighted imaging in the differential diagnosis of ovarian lesions: a meta-analysis. PLoS One 2016; 11: e0149465. doi: 10.1371/journal.pone.0149465.
    1. Pi S, Cao R, Qiang JW, Guo YH. Utility of DWI with quantitative ADC values in ovarian tumors: a meta-analysis of diagnostic test performance. Acta Radiol 2018; 59: 1386-1394.
    1. Wang T, Li W, Wu X, et al. . Tubo-ovarian abscess (with/without pseudotumor area) mimicking ovarian malignancy: role of diffusion-weighted MR imaging with apparent diffusion coefficient values. PLoS One 2016; 11: e0149318. doi: 10.1371/journal.pone.0149318.
    1. Chou CP, Chiou SH, Levenson RB, et al. . Differentiation between pelvic abscesses and pelvic tumors with diffusion-weighted MR imaging: a preliminary study. Clin Imaging 2012; 36: 532-538.
    1. Timmerman D, Ameye L, Fischerova D, et al. . Simple ultrasound rules to distinguish between benign and malignant adnexal masses before surgery: prospective validation by IOTA group. BMJ 2010; 341: c6839. doi: 10.1136/bmj.c6839.
    1. Foti PV, Ognibene N, Spadola S, et al. . Non-neoplastic diseases of the fallopian tube: MR imaging with emphasis on diffusion-weighted imaging. Insights Imaging 2016; 7: 311-327.
    1. Bilgin T, Karabay A, Dolar E, Develioğlu OH. Peritoneal tuberculosis with pelvic abdominal mass, ascites and elevated CA 125 mimicking advanced ovarian carcinoma: a series of 10 cases. Int J Gynecol Cancer 2001; 11: 290-294.
    1. Kim SH, Kim SH, Yang DM, Kim KA. Unusual causes of tubo-ovarian abscess: CT and MR imaging findings. Radiographics 2004; 24: 1575-1589.
    1. Imaoka I, Wada A, Kaji Y, et al. . Developing an MR imaging strategy for diagnosis of ovarian masses. Radiographics 2006; 26: 1431-1448.
    1. Castillo M, Mukherji SK. Diffusion-weighted imaging in the evaluation of intracranial lesions. Semin Ultrasound CT MR 2000; 21: 405-416.
    1. Chiang IC, Hsieh TJ, Chiu ML, Liu GC, Kuo YT, Lin WC. Distinction between pyogenic brain abscess and necrotic brain tumour using 3-tesla MR spectroscopy, diffusion and perfusion imaging. Br J Radiol 2009; 82: 813-820.
    1. Chan JH, Tsui EY, Luk SH, et al. . Diffusion-weighted MR imaging of the liver: distinguishing hepatic abscess from cystic or necrotic tumor. Abdom Imaging 2001; 26: 161-165.
    1. Tantawy MSI, Elrakhawy MM, El-Morsy A, et al. . DWI in characterization of complex ovarian masses, would it help? The Egyptian Journal of Radiology and Nuclear Medicine 2018 ; 49: 878-883.
    1. Fujii S, Kakite S, Nishihara K, et al. . Diagnostic accuracy of diffusionweighted imaging in differentiating benign from malignant ovarian lesions. J Magn Reson Imaging 2008; 28: 1149-1156.
    1. Nakayama T, Yoshimitsu K, Irie H, et al. . Diffusion-weighted echoplanar MR imaging and ADC mapping in the differential diagnosis of ovarian cystic masses: usefulness of detecting keratinoid substances in mature cystic teratomas. J Magn Reson Imaging 2005; 22: 271-278.
    1. Holzapfel K, Rummeny E, Gaa J. Diffusion-weighted MR imaging of hepatic abscesses: possibility of different apparent diffusion coefficient (ADC)-values in early and mature abscess formation. Abdom Imaging 2007; 32: 538-539.
    1. Unal O, Koparan HI, Avcu S, Kalender AM, Kisli E. The diagnostic value of diffusion-weighted magnetic resonance imaging in soft tissue abscesses. Eur J Radiol 2011; 77: 490-494.
    1. Ueda H, Togashi K, Kataoka ML, et al. . Adnexal masses caused by pelvic inflammatory disease: MR appearance. Magn Reson Med Sci 2002; 1: 207-215.
    1. Qayyum A. Diffusion-weighted imaging in the abdomen and pelvis: concepts and applications. Radiographics 2009; 29: 1797-1810.
    1. Orton MR, Messiou C, Collins D, et al. . Diffusion-weighted MR imaging of metastatic abdominal and pelvic tumours is sensitive to early changes induced by a VEGF inhibitor using alternative diffusion attenuation models. Eur Radiol 2016; 26: 1412-1419.

Source: PubMed

3
Se inscrever