Short
Communication
In
our preliminary study we propose the first multiparametric MRI classification
of renal suspicious lesions: KI-RADS (Kidney Imaging Reporting and Data
System).
There
are currently other RADS criteria used in clinical practice for other anatomic
districts such as breast (BI-RADS- Breast Imaging Reporting and Data System),
colon (C-RADS-Colon Imaging Reporting and Data System), liver (LI-RADS-Liver
Imaging Reporting and Data System), lung (Lung-RADS-Lung Imaging Reporting and
Data System), head and neck (NI-RADS-Head and Neck Imaging Reporting and Data
System), adnexal (O-RADS-Adnexal Imaging Reporting and Data System), prostate
(PI-RADS-Prostate Imaging Reporting and Data System), thyroid (TI-RADS- Thyroid
Imaging Reporting and Data System) and coronary artery disease (CAD-RADS-Coronary
Artery Disease Imaging Reporting And Data System).
Similar
to the PI-RADS criteria our classification is based on multiparametric MRI.
Furthermore,
our classification not only provides a standardized score on the severity of
renal suspicious lesions, but offers a simple surgical score that communicates
to urologists the preoperative planning in a rapid manner.
Our
KI-RADS criteria integrate the existing Computed Tomography (CT) renal
malignancy criteria as well as the Bosniak criteria (for the evaluation of
renal cystic complex lesions). In Resonance Magnetic Imaging (MRI) we consider
a suspicious renal lesion based on the contemporary evaluation of these three
parameters: T2 morphological sequences, diffusion (DWI/ADC) sequences and
perfusion sequences (contrast enhancement).
Diagnosing
kidney cancer through Imaging, especially in its early stages, is always a
challenge. It is often identified incidentally when the patient undergoes a Computed
Tomography (CT) or Magnetic Resonance Imaging (MRI) scan for other reasons. It
usually becomes clinically evident very late. Furthermore, the nature of a
renal lesion is often diagnosed only after surgery (nephrectomy or
enucleoresection).
On
Imaging renal cancer can present in various ways. It can be exophytic or
intraparenchymal. There is no size criterion to predict malignancy. The margins
of the lesion can be regular or irregular. It could present a solid or mixed
solid-cystic structure. It can be highly or poorly vascularized. It can be a
homogeneous or heterogeneous lesion (with internal necrotic areas). On MRI
regardless of the size of the lesion, the regularity or irregularity of the
margins and whether or not intralesional homogeneity is present (on T2 images)
any suspicious renal lesion presents a T2 signal that is often intermediate
compared to the renal cortex (often associated with irregular margin and
intralesional inhomogeneity), diffusion positivity/restriction (high signal in
DWI and low in ADC) and contrast enhancement (that is often not homogeneous).
In T2 sequences we can exclude with certainty only the presence of a simple renal
cyst. A renal lesion is suspicious when it presents a solid component in T2
images (usually intermediate signal), positivity/restriction in diffusion
(DWI/ADC) images and contrast enhancement in perfusion sequences. In this way,
to consider a renal lesion suspicious, we simultaneously evaluate the
morphology of the mass (or nodule) in the T2 sequence, the diffusion positivity
and the presence of intralesional contrast enhancement.
Furthermore, T2 sequences have an excellent contrast resolution to perfectly differentiate the renal cortex (intermediate signal) from the renal pelvis (high signal). Starting from this assumption we consider as in figure 1.
Figure 1: KI-RADS- Kidney Imaging Reporting and Data System assumption size as follows
KI-RADS
1: Any suspicious lesion in multiparametric assessment (of any size) with
invasion of the renal cortex less than 5 mm
KI-RADS
2: Any suspicious lesion in multiparametric assessment (of any size) with
invasion of the renal cortex more than 5 mm
KI-RADS
3: Any suspicious lesion in multiparametric assessment (of any size) borderline
beetwin cortical and renal pelvis
KI-RADS
4: Any suspicious lesion in multiparametric assessment (of any size) with
invasion of the renal pelvis less than 5 mm
KI-RADS
5: Any suspicious lesion in multiparametric assessment (of any size) with
invasion of the renal pelvis more than 5 mm
According to this classification, KI-RADS lesions 1 and 2 are suspicious lesions that usually undergo surgical enucleoresection (surgical technique), while KI-RADS lesions 3, 4 and 5 are suspicious lesions that undergo total nephrectomy.
Our preliminary study is still in its infancy and requires further data and future investigations. It is certainly an innovative, standardized and practical approach to interpreting the renal lesions. It certainly offers a preliminary advantage to urologists in the preoperative planning of renal masses. It is also well suited for surgical evaluation after chemotherapy and immunotherapy.