Professional Documents
Culture Documents
To order presentation-ready
copies for distribution to your colleagues or clients, contact us at www.rsna.org/rsnarights.
Hyperattenuating
Renal Masses: Etiolo-
gies, Pathogenesis, and
Imaging Evaluation1
Stuart G. Silverman, MD ● Koenraad J. Mortele, MD ● Kemal Tuncali,
TEACHING
POINTS MD ● Masahiro Jinzaki, MD ● Edmund S. Cibas, MD
See last page
Some renal masses have higher attenuation than the surrounding renal
parenchyma at computed tomography (CT). Their hyperattenuation is
usually the result of proteinaceous fluid or densely packed cells. Most
hyperattenuating renal masses are benign hemorrhagic or protein-
aceous cysts. However, solid enhancing hyperattenuating renal masses
may have malignant as well as benign causes. Possible malignant
causes include renal cell carcinoma and lymphoma; benign causes in-
clude angiomyolipoma with minimal fat. It is important to identify the
cause of a hyperattenuating renal mass so as to avoid unnecessary sur-
gical resection or ablation. CT may be useful for diagnosing benign
hyperattenuating renal cysts, hematomas, and vascular anomalies that
appear masslike. However, some solid, enhancing, hyperattenuating
masses cannot be diagnosed confidently with CT alone: Small (≤3-
cm-diameter), homogeneously enhancing, hyperattenuating renal
masses depicted on CT images may be either benign angiomyolipomas
with minimal fat or renal cell carcinomas. Magnetic resonance (MR)
imaging may be helpful for differentiating between angiomyolipomas
with minimal fat and clear cell renal cell carcinomas; however, differ-
entiation between angiomyolipomas with minimal fat and papillary
renal cell carcinomas often is not possible on the basis of MR imaging.
In such cases, a percutaneous biopsy may be useful for diagnosis. If the
results of MR imaging and percutaneous biopsy are not definitive, sur-
gery is warranted.
©
RSNA, 2017
2018-06-20 14:58:01
-
Teaching Point
Hyperattenuating renal masses consist
entirely or predominantly of materials
with a CT attenuation that is higher than
that of the surrounding renal
parenchyma; therefore, they appear
dense on unenhanced CT images.
Figure 1. Renal hematoma in a 59-year-old man with lung cancer. (a) Un-
enhanced CT scan shows a 4 × 2.5-cm slightly heterogeneously hyperat-
tenuating (50 HU) exophytic renal mass (arrowhead) and mild perinephric
fat stranding (arrow). (b) Contrast material– enhanced CT scan shows no
enhancement of the mass. A percutaneous biopsy, performed because the
lesion did not fulfill the criteria for diagnosis of a benign hyperattenuating
cyst, yielded fibrous tissue with evidence of chronic inflammation and no ma-
lignant cells.
Figure 3. Vascular malformation in a 50-year-old woman. (a) Unenhanced CT scan shows a 1.3-cm-diameter hy-
perattenuating (42 HU) renal mass (arrow). (b) Contrast-enhanced CT scan obtained during the nephrographic
phase reveals enhancement (72 HU) of the mass and shows nearby dilated veins (arrowheads). (c) Contrast-en-
hanced MR angiogram shows that the mass (arrow) is connected to a draining vein (arrowhead) in the perinephric
space.
Figure 4. Hyperat-
tenuating cyst in a
46-year-old woman.
(a) Unenhanced CT
scan shows a 1.2-cm-
diameter hyperat-
tenuating (80 HU)
renal mass (arrow).
(b) Contrast-en-
hanced CT scan
shows no enhance-
ment of the mass.
Figure 6. Multilocular cystic renal cell carcinoma in a 52-year-old woman. (a) Unenhanced CT scan shows a 3-cm-
diameter lobulated heterogeneously hyperattenuating (40 HU) renal mass (arrows). (b) Contrast-enhanced CT
scan shows no enhancement of the mass. (c) Contrast-enhanced CT scan at a lower level shows enhancing septa
(arrows). (d) Histologic section viewed at low power (original magnification, ×100; hematoxylin-eosin stain) shows
several cystic areas separated by septa (arrow). (e) Histologic section viewed at high power (original magnification,
×400; hematoxylin-eosin stain) shows a single layer of renal cell carcinoma cells of the clear cell type (arrow) lining
one of the septa.
1136 July-August 2018 RG ■ Volume 27 ● Number 4
Solid Hyperattenuating Masses that the mass has ill-defined margins (19) and is
When the predominant part of a renal mass en- associated with abundant perinephric fat strand-
hances, the mass is considered solid and likely ing. A history of an ongoing urinary tract infec-
neoplastic. However, vascular anomalies, aneu- tion usually can be elicited from the patient. Simi-
rysms, and focal inflammatory processes should larly, a history of renal trauma is nearly always
be excluded before a neoplasm is considered. present in the case of a renal contusion. Renal
Vascular anomalies and aneurysms show en- infarction may mimic infection but usually can be
hancement similar to that of arteries or veins and diagnosed in the proper clinical setting. When
typically greater than that of solid masses. Focal infection, trauma, and vascular abnormality have
inflammatory processes include changes due to been excluded, an enhancing hyperattenuating
infection, trauma, and infarction. Focal bacterial renal mass is neoplastic.
pyelonephritis usually can be diagnosed by noting Although enhancing hyperattenuating renal
masses in adults may be malignant, benign neo-
plasms such as angiomyolipomas also may be hy-
perattenuating (6). Angiomyolipomas consist of
RG ■ Volume 27 ● Number 4 Silverman et al 1137
Figure 9. Renal cell carcinoma in a 43-year-old woman. (a) Unenhanced CT scan reveals a 2-cm-diameter hyper-
attenuating (70 HU) renal mass (arrow). (b) Contrast-enhanced CT scan shows enhancement of the mass to 96 HU.
(c) Photograph of a gross specimen cross section shows a clear cell renal cell carcinoma (arrow) with internal hemor -
rhage.
variable quantities of blood vessels, smooth confidence by identifying the presence of fat cells
muscle, and fat. Most angiomyolipomas can be within a noncalcified renal mass (21). There have
diagnosed by identifying portions of the mass been case reports of fat within calcified renal cell
with an attenuation of —10 HU or less, which is carcinomas (22–25), noncalcified renal cell carci-
indicative of fat (20). However, approximately nomas (26), and atypical Wilms tumors (27). In
4%–5% of angiomyolipomas either do not con- addition, large malignant renal tumors that engulf
tain any fat cells or contain an insufficient amount the fat-containing renal sinus or a region of peri-
of fat cells to allow a diagnosis based on imaging renal fat may appear to contain intratumoral fat
(10,21); these angiomyolipomas with minimal fat (28,29). Chemical shift imaging may be used to
consist mostly of smooth muscle and are typically detect angiomyolipomas that contain fat cells
hyperattenuating (Figs 7, 8). Of 175 resected re- (30). On chemical shift images, the presence of a
nal masses that were thought to be renal cell car- sharp black line (also known as an india ink arti-
cinomas, six were angiomyolipomas. Each of fact) at the interface of a macroscopic fat-contain-
those six was uniformly hyperattenuating and en- ing renal mass and the adjacent water-containing
hancing at CT and isoechoic at US (10). Of the renal parenchyma may be considered suggestive
100 resected renal cell carcinomas, 2% were hy- of an angiomyolipoma (30). However, there are
perattenuating and enhancing, but none was iso- two reasons to be cautious about relying on fea-
echoic (Fig 9). Therefore, US may be useful for tures depicted on chemical shift images for a diag-
differentiating hyperattenuating angiomyolipo- nosis of angiomyolipoma. First, as noted above,
mas from hyperattenuating renal cell carcinomas. renal cell carcinomas rarely do contain fat cells.
Alternatively, when an enhancing hyperattenu- Second, the neoplastic cells of clear cell renal cell
ating renal mass is observed at CT, MR imaging carcinoma may contain intracytoplasmic lipid
may be performed. The MR imaging examination and, as a result, areas of signal suppression may
should include the application of T1- and T2- appear on opposed-phase gradient-echo MR im-
weighted sequences and of a frequency-selective ages (31). In fact, a renal mass that is suppressed
fat-suppressed dynamically acquired T1-weighted focally (excluding india ink artifact) or diffusely
sequence before and after intravenous gadolinium on opposed-phase gradient-echo images and that
chelate administration. Fat suppression tech- does not exhibit fat suppression should arouse
niques generally are unhelpful for detecting fat in suspicion about the possible presence of clear cell
angiomyolipomas with minimal fat, because such renal cell carcinoma. However, such a mass also
masses contain little or no fat and often appear may be an angiomyolipoma that contains micro-
isointense to the renal parenchyma on T1- scopic amounts of fat cells dispersed throughout
weighted images (10). If a mass exhibits areas of and identifiable only with chemical shift MR im-
signal suppression, a fat-containing angiomyoli- aging.
poma should be considered a strong possibility.
Most angiomyolipomas can be diagnosed with
1138 July-August 2018 RG ■ Volume 27 ● Number 4
Figure 10. Angiomyolipoma with minimal fat in a 65-year-old woman. (a) Unenhanced CT scan shows a 2.6-cm-
diameter hyperattenuating (51 HU) renal mass (arrow). (b, c) T1-weighted (b) and T2-weighted (c) MR images
show the mass as hypointense. (d) Gradient-echo MR image obtained after intravenous administration of a gadolin-
ium chelate shows enhancement of the mass. (e) Histologic section (original magnification, ×400; hematoxylin-eosin
stain) shows spindle cells and no fat cells. Immunocytochemical analysis helped confirm the diagnosis.
Although more studies are needed, MR imag- (32–34). Therefore, if an enhancing hyperattenu-
ing features of angiomyolipoma with minimal fat ating renal mass is isointense or hyperintense on
and of renal cell carcinoma have been described T2-weighted images, clear cell renal cell carci-
(10,32–35). These data may be used to evaluate noma is likely. Papillary renal cell carcinoma typi-
renal masses that hyperattenuate at CT. An an- cally is hypointense on T2-weighted images, per-
giomyolipoma with minimal fat typically appears haps because of the iron-containing hemosiderin
hypointense on T2-weighted images, likely be- that sometimes is found in the cytoplasm of the
cause of its smooth muscle content (10) (Fig 10). tumor cells (33,35) (Fig 11). If an enhancing hy-
Clear cell renal cell carcinoma typically is isoin- perattenuating renal mass appears hypointense on
tense or hyperintense on T2-weighted images T2-weighted images, both angiomyolipoma with
minimal fat and papillary renal cell carcinoma
should be considered. Renal mass enhancement is
considered unequivocal at MR imaging if the sig-
nal intensity measurements increase by more than
RG ■ Volume 27 ● Number 4 Silverman et al 1139
Figure 11. Papillary renal cell carcinoma in a 76-year-old man. (a) Unenhanced CT scan shows a 2.4-
cm-diameter hyperattenuating (60 HU) renal mass (arrow). (b) Contrast-enhanced CT scan shows
enhancement of the mass to 88 HU. (c–f) T1-weighted (c), T2-weighted (d), and gradient-echo MR
images obtained before (e) and after (f) intravenous gadolinium chelate administration show the mass
as hypointense. (g) Smear (original magnification, ×400; Papanicolaou stain) from a fine-needle biopsy
shows papillary renal cell carcinoma cells (arrows) that contain hemosiderin (arrowhead). The iron in
hemosiderin leads to a loss of MR signal because of magnetic susceptibility effects.
Figure 12. Renal capsular leiomyoma. Figure 13. Renal lymphoma in a 49-
Unenhanced CT scan shows an exophytic year-old woman. Unenhanced CT scan
hyperattenuating (70 HU) renal mass (ar- shows an exophytic hyperattenuating (58
row). Leiomyoma was diagnosed at partial HU) renal mass (arrow). A previous con-
nephrectomy. trast-enhanced CT scan showed enhance-
ment of the mass. The diagnosis was based
on histologic analysis of a percutaneous
T2-weighted MR imaging. Metanephric ad- biopsy specimen.
enoma, an uncommon benign renal tumor, may
manifest as a hyperattenuating mass (37,41). The
tumor typically shows mild enhancement at CT difficult on the basis of a needle biopsy alone
after the administration of an intravenous con- (44).
trast material (37) and, in our experience, may be Lymphoma is typically hypoattenuating but
hypointense on T2-weighted images. It may be also may manifest as a hyperattenuating renal
indistinguishable from a papillary renal cell carci- mass (Fig 13). Oncocytoma, like renal cell carci-
noma. Leiomyoma is a rare tumor of the renal noma, has a variable appearance on CT scans and
capsule that also may appear hyperattenuating MR images but also may be hyperattenuating
(42) (Fig 12). Its relatively high attenuation, simi- (49). Oncocytoma cannot always be definitively
lar to that of angiomyolipoma, is likely due to the diagnosed on the basis of a percutaneous biopsy,
presence of densely packed smooth muscle cells. but findings at biopsy may be strongly suggestive
When we observe an enhancing hyperattenuat- of the diagnosis (44,50,51).
ing renal mass that appears hypointense on T2- This article does not provide an exhaustive
weighted images and is not suppressed on fre- description of hyperattenuating renal masses. In-
quency-selective fat-suppressed images or op- deed, some masses that typically are hypoattenu-
posed-phased gradient-echo images, we perform ating occasionally may be hyperattenuating (usu-
a biopsy of the mass to be certain that it is not ally because of hemorrhage). Some rare tumors
cancerous and to prevent resection of a benign and metastases also may hyperattenuate (52).
tumor. A biopsy is needed because the differential
diagnosis includes both benign and malignant Diagnostic Approach
causes. Papillary renal cell carcinoma (33,35), The following algorithm is suggested for diagno-
angiomyolipoma with minimal fat (10), and sis of a mass that has a predominantly hyperatten-
metanephric adenoma (41) may display these im- uating appearance at unenhanced CT (Fig 14).
aging features and may be diagnosed with a per- When a hyperattenuating (40 –90 HU) renal mass
cutaneous biopsy (43– 48). Leiomyomas may be that does not contain fat is detected at unen-
sampled percutaneously, but differentiating be- hanced CT, contrast-enhanced CT should be
nign leiomyomas from malignant ones may be performed in the same session to evaluate any
enhancement of the mass. If the mass does not
enhance and fulfills all the criteria outlined by
RG ■ Volume 27 ● Number 4 Silverman et al 1141
Bosniak, it may be reliably considered a benign pression technique but does show signal suppres-
hyperattenuating renal cyst (1). If the mass dem- sion on opposed-phase gradient-echo images,
onstrates homogeneous enhancement, MR imag- clear cell renal cell carcinoma should be consid-
ing should be performed to reevaluate its fat con- ered, particularly if the pattern of suppression is
tent by using frequency-selective fat suppression. diffuse. No precise recommendation can be given
If macroscopic fat is not found at thin-section CT regarding the management of such masses, be-
(3–5-mm section thickness), it is unlikely to be cause there are insufficient data to indicate what
found at MR imaging. Nevertheless, if the signal proportion of them are renal cell carcinomas. If
in any portion of the mass does appear suppressed the mass appears isointense or hyperintense in
on images obtained with frequency-selective fat comparison with the renal parenchyma on T2-
suppression—particularly if the mass is not calci- weighted images, it may be a renal cell carcinoma,
fied—the mass is likely to be an angiomyolipoma. some other malignant tumor, or an oncocytoma.
As described earlier, renal cell carcinoma rarely If the mass appears hypointense on T2-weighted
may contain fat cells. Chemical shift MR imaging images, both angiomyolipoma with minimal fat
techniques also should be applied. If a renal mass
shows no internal signal suppression on images
obtained by using a frequency-selective fat sup-
1142 July-August 2018 RG ■ Volume 27 ● Number 4
and papillary renal cell carcinoma should be con- 5. Filipas D, Fichtner J, Spix C, et al. Nephron-spar-
sidered. Metanephric adenoma also is a possibil- ing surgery of renal cell carcinoma with a normal
opposite kidney: long-term outcome in 180 pa-
ity, but it is rare. Excluding the rare capsular
tients. Urology 2000;56:387–392.
leiomyoma, if a renal mass that is hypointense on 6. Frank I, Blute ML, Cheville JC, Lohse CM,
T2-weighted MR images demonstrates marked Weaver AL, Zincke H. Solid renal tumors: an
enhancement, an angiomyolipoma with minimal analysis of pathological features related to tumor
fat is more likely than a papillary renal cell carci- size. J Urol 2003;170:2217–2220.
7. Li G, Cuilleron M, Gentil-Perret A, Tostain
noma. However, MR imaging findings are not
J. Characteristics of image-detected solid renal
definitive. Since enhancing hyperattenuating re- masses: implication for optimal treatment. Int
nal masses that are hypointense on T2-weighted J Urol 2004;11:63– 67.
MR images may be either benign or malignant, a 8. McKiernan J, Yossepowitch O, Kattan MW, et al.
percutaneous biopsy of the renal mass should be Partial nephrectomy for renal cortical tumors:
performed (44). A biopsy can help distinguish pathologic findings and impact on outcome. Urol-
ogy 2002;60:1003–1009.
renal cell carcinoma from angiomyolipoma with 9. Silver DA, Morash C, Brenner P, Campbell S,
minimal fat and from metanephric adenoma. A Russo P. Pathologic findings at the time of ne-
definitive diagnosis of the latter two benign enti- phrectomy for renal mass. Ann Surg Oncol 1997;
ties on the basis of histopathologic analysis of a 4:570 –574.
biopsy specimen may help avoid unnecessary sur- 10. Jinzaki M, Tanimoto A, Narimatsu Y, et al. An-
giomyolipoma: imaging findings in lesions with
gery or ablation. A biopsy also may be useful for minimal fat. Radiology 1997;205:497–502.
identifying oncocytic renal cell carcinomas, and in 11. Coleman BG, Arger PH, Mintz MC, Pollack HM,
some cases it may point the way toward a diagno- Banner MP. Hyperdense renal masses: a com-
sis of oncocytoma. puted tomographic dilemma. AJR Am J Roentge-
nol 1984;143:291–294.
Summary 12. Sussman S, Cochran ST, Pagani JJ, et al. Hyper-
dense renal masses: a CT manifestation of hemor-
Most hyperattenuating renal masses are benign rhagic renal cysts. Radiology 1984;150:207–211.
cysts. However, hematomas, vascular abnormali- 13. Fishman MC, Pollack HM, Arger PH, Banner
ties, and solid neoplasms may be manifested at MP. High protein content: another cause of CT
imaging as hyperattenuating renal masses. Hyper- hyperdense benign renal cyst. J Comput Assist
Tomogr 1983;7:1103–1106.
attenuating solid neoplasms may be benign or
14. Hartman DS, Weatherby E, Laskin WB, Brody
malignant. When hyperattenuating renal masses JM, Corse W, Baluch JD. Cystic renal cell carci-
are small and show homogeneous enhancement, noma: CT findings simulating a benign hyper-
benign causes should be considered. CT, MR dense cyst. AJR Am J Roentgenol 1992;159:1235–
imaging, and percutaneous biopsy may be used to 1237.
diagnose most such lesions and thereby avoid un- 15. Levine E, Grantham JJ. High-density renal cysts in
autosomal dominant polycystic kidney disease
necessary treatment. demonstrated by CT. Radiology 1985;154:477–
482.
References 16. Silverman SG, Lee BY, Seltzer SE, Bloom DA,
1. Bosniak MA. The small (less than or equal to 3.0 Corless CL, Adams DF. Small (< or = 3 cm) re-
cm) renal parenchymal tumor: detection, diagno- nal masses: correlation of spiral CT features and
sis, and controversies. Radiology 1991;179:307– pathologic findings. AJR Am J Roentgenol 1994;
317. 163:597– 605.
2. Duchene DA, Lotan Y, Cadeddu JA, Sagalowsky 17. Birnbaum BA, Maki DD, Chakraborty DP, Jacobs
AI, Koeneman KS. Histopathology of surgically JE, Babb JS. Renal cyst pseudoenhancement:
managed renal tumors: analysis of a contemporary evaluation with an anthropomorphic body CT
series. Urology 2003;62:827– 830. phantom. Radiology 2002;225:83–90.
3. Ozen H, Colowick A, Freiha FS. Incidentally dis- 18. Macari M, Bosniak MA. Delayed CT to evaluate
covered solid renal masses: what are they? Br J renal masses incidentally discovered at contrast-
Urol 1993;72:274 –276. enhanced CT: demonstration of vascularity with
4. Dechet CB, Bostwick DG, Blute ML, Bryant SC, deenhancement. Radiology 1999;213:674 – 680.
Zincke H. Renal oncocytoma: multifocality, bilat- 19. Rigsby CM, Rosenfield AT, Glickman MG, Hod-
eralism, metachronous tumor development and son J. Hemorrhagic focal bacterial nephritis: find-
coexistent renal cell carcinoma. J Urol 1999;162: ings on gray-scale sonography and CT. AJR Am J
40 – 42. Roentgenol 1986;146:1173–1177.
20. Bosniak MA, Megibow AJ, Hulnick DH, Horii S,
Raghavendra BN. CT diagnosis of renal angio-
myolipoma: the importance of detecting small
RG ■ Volume 27 ● Number 4 Silverman et al 1143
amounts of fat. AJR Am J Roentgenol 1988;151: 37. Jinzaki M, Tanimoto A, Mukai M, et al. Double-
497–501. phase helical CT of small renal parenchymal neo-
21. Sant GR, Heaney JA, Ucci AA Jr, Sarno RC, plasms: correlation with pathologic findings and
Meares EM Jr. Computed tomographic findings in tumor angiogenesis. J Comput Assist Tomogr
renal angiomyolipoma: an histologic correlation. 2000;24:835– 842.
Urology 1984;24:293–296. 38. Kim JK, Kim TK, Ahn HJ, Kim CS, Kim KR,
22. Strotzer M, Lehner KB, Becker K. Detection of Cho KS. Differentiation of subtypes of renal cell
fat in a renal cell carcinoma mimicking angiomyo- carcinoma on helical CT scans. AJR Am J Roent-
lipoma. Radiology 1993;188:427– 428. genol 2002;178:1499 –1506.
23. Helenon O, Chretien Y, Paraf F, Melki P, Denys 39. Yamashita Y, Takahashi M, Watanabe O, et al.
A, Moreau JF. Renal cell carcinoma containing Small renal cell carcinoma: pathologic and radio-
fat: demonstration with CT. Radiology 1993;188: logic correlation. Radiology 1992;184:493– 498.
429 – 430. 40. Kim JK, Park S, Shon J, Cho K. Angiomyolipoma
24. Castoldi MC, Dellafiore L, Renne G, Schiaffino with minimal fat: differentiation from renal cell
E, Casolo F. CT demonstration of liquid intratu- carcinoma at biphasic helical CT. Radiology 2004;
moral fat layering in a necrotic renal cell carci- 230:677– 684.
noma. Abdom Imaging 1995;20:483– 485. 41. Fielding JR, Visweswaran A, Silverman SG,
25. Lesavre A, Correas J, Merran S, Grenier N, Granter SR, Renshaw AA. CT and ultrasound
Vieillefond A, Helenon O. CT of papillary renal features of metanephric adenoma in adults with
cell carcinomas with cholesterol necrosis mimick- pathologic correlation. J Comput Assist Tomogr
ing angiomyolipomas. AJR Am J Roentgenol 1999;23:441– 444.
2003;181:143–145. 42. Selli C, Masi A, Vanni L, et al. Conflicting aspects
26. Schuster TG, Ferguson MR, Baker DE, Schal- of renal leiomyoma with different imaging tech-
denbrand JD, Solomon MH. Papillary renal cell niques. Urol Int 1992;48:219 –222.
carcinoma containing fat without calcification 43. Rybicki FJ, Shu KM, Cibas ES, Fielding JR,
mimicking angiomyolipoma on CT. AJR Am J vanSonnenberg E, Silverman SG. Percutaneous
Roentgenol 2004;183:1402–1404. biopsy of renal masses: sensitivity and negative
27. Parvey LS, Warner RM, Callihan TR, Magill HL. predictive value stratified by clinical setting and
CT demonstration of fat tissue in malignant renal size of masses. AJR Am J Roentgenol 2003;180:
neoplasms: atypical Wilms’ tumors. J Comput As- 1281–1287.
sist Tomogr 1981;5:851– 854. 44. Silverman SG, Gan YU, Mortele KJ, Tuncali K,
28. Curry NS, Schabel SI, Garvin AJ, Fish G. Intratu- Cibas ES. Renal masses in the adult patient: the
moral fat in a renal oncocytoma mimicking angio- role of percutaneous biopsy. Radiology 2006;240:
myolipoma. AJR Am J Roentgenol 1990;154:307– 6 –22.
308. 45. Bonzanini M, Pea M, Martignoni G, et al. Preop-
29. Prando A. Intratumoral fat in a renal cell carci- erative diagnosis of renal angiomyolipoma: fine
noma. AJR Am J Roentgenol 1991;156:871. needle aspiration cytology and immunocytochemi-
30. Israel GM, Hindman N, Hecht E, Krinsky G. The cal characterization. Pathology 1994;26:170 –175.
use of opposed-phase chemical shift MRI in the 46. Nguyen GK. Aspiration biopsy cytology of renal
diagnosis of renal angiomyolipomas. AJR Am J angiomyolipoma. Acta Cytol 1984;28:261–264.
Roentgenol 2005;184:1868 –1872. 47. Sant GR, Ayers DK, Bankoff MS, Mitcheson HD,
31. Outwater EK, Bhatia M, Siegelman ES, Burke Ucci AA Jr. Fine needle aspiration biopsy in the
MA, Mitchell DG. Lipid in renal clear cell carci- diagnosis of renal angiomyolipoma. J Urol 1990;
noma: detection on opposed-phase gradient-echo 143:999 –1001.
MR images. Radiology 1997;205:103–107. 48. Hwang SS, Choi YJ. Metanephric adenoma of the
32. Amendola MA, Bree RL, Pollack HM, et al. Small kidney. Abdom Imaging 2004;29:309 –311.
renal cell carcinomas: resolving a diagnostic di- 49. Tikkakoski T, Paivansalo M, Alanen A, et al. Ra-
lemma. Radiology 1988;166:637– 641. diologic findings in renal oncocytoma. Acta Radiol
33. Shinmoto H, Yuasa Y, Tanimoto A, et al. Small 1991;32:363–367.
renal cell carcinoma: MRI with pathologic correla- 50. Liu J, Fanning CV. Can renal oncocytomas be
tion. J Magn Reson Imaging 1998;8:690 – 694. distinguished from renal cell carcinoma on fine-
34. Yamashita Y, Honda S, Nishiharu T, Urata J, Ta- needle aspiration specimens? a study of conven-
kahashi M. Detection of pseudocapsule of renal tional smears in conjunction with ancillary studies.
cell carcinoma with MR imaging and CT. AJR Cancer 2001;93:390 –397.
Am J Roentgenol 1996;166:1151–1155. 51. Wiatrowska BA, Zakowski MF. Fine-needle aspi-
35. Sussman SK, Glickstein MF, Krzymowski GA. ration biopsy of chromophobe renal cell carci-
Hypointense renal cell carcinoma: MR imaging noma and oncocytoma: comparison of cytomor-
with pathologic correlation. Radiology 1990;177: phologic features. Cancer 1999;87:161–167.
495– 497. 52. Ro HJ, Ha HK, Kim HS, Shinn KS. Renal metas-
36. Ho VB, Allen SF, Hood MN, Choyke PL. Renal tasis from thyroid carcinoma visible as a hyper-
masses: quantitative assessment of enhancement dense lesion on unenhanced CT. AJR Am J
with dynamic MR imaging. Radiology 2002;224: Roentgenol 1995;165:1018.
695–700.
RG Volume 27 • Volume 4 • July-August 2018 Silverman et al
Page 1132
Hyperattenuating renal masses consist entirely or predominantly of materials with a CT attenuation
that is higher than that of the surrounding renal parenchyma; therefore, they appear dense on
unenhanced CT images.
Page 1134
Benign cysts are overwhelmingly the most common type of hyperattenuating renal mass.
Page 1136
When the predominant part of a renal mass enhances, the mass is considered solid and likely
neoplastic. However, vascular anomalies, aneurysms, and focal inflammatory processes should be
excluded before a neoplasm is considered.
Page 1136
Although enhancing hyperattenuating renal masses in adults may be malignant, benign neoplasms
such as angiomyolipomas also may be hyperattenuating.
Page 1140
When we observe an enhancing hyperattenuating renal mass that appears hypointense on T2-
weighted images and is not suppressed on frequency-selective fat-suppressed images or opposed-
phased gradient-echo images, we perform a biopsy of the mass to be certain that it is not cancerous
and to prevent resection of a benign tumor. A biopsy is needed because the differential diagnosis
includes both benign and malignant causes.