carcinoma de celulas renales y diferenciales en métodos diagnósticos de imagen
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carcinoma de celulas renales y diferenciales en métodos diagnósticos de imagenTRANSCRIPT
D R A . M A R I A A N T O N I E T A R A M O SK A R E N M E Z A
CARCINOMA DE CÉLULAS RENALES (CCR)
Grupo 5.4matrícula: 259943
RRC
RRC
malignant tumours derived from the renal
epithelium
most common malignant renal
tumour
variety of radiographic appearances
Epidemiology
50-70 years of age at
presentation
male predilection
of 2:1
Clinical presentation
macroscopic hematuria:
60%
flank pain: 40%
palpable flank mass:
30-40%
This triad is however only found in 10-15% of patients
RISK FACTORS
obesity
dialysis
cigarette smoking
PARANEOPLASIC SYNDROMES
Polycythaemia
Hypercalcaemia
Stauffer syndrome
Robson staging: *stage I - limited to kidney*stage II - involvement of perinephric fat but remains limited to Gerota's fascia*stage III IIIa - renal vein involvement IIIb - nodal involvement IIIc - both IIIa and IIIb*stage IV IVa - direct invasion of adjacent organs / structures IVb - distant metastases
CTUSED TO BOTH DIAGNOSE AND STAGE RENAL CELL CARCINOMAS
On non-contrast CT the lesions appear of soft
tissue attenuation
Approximately 30% demonstrate some calcification
In general small lesions enhance homogeneously
Larger lesions have irregular
enhancement due to areas of necrosis
MRIIS ALSO ABLE TO SUGGEST THE LIKELY HISTOLOGY, ON THE GROUNDS OF
T2 DIFFERENCES
MR
IT1 - often heterogeneous due to necrosis, haemorrhage and solid
components
T2 - appearances depend on histology 6
clear cell RCC - hyper intensepapillary RCC - hypo intense
MRI
Tumour pseudocapsule appears as an
hypointense rim between the tumor and
the adjacent parenchyma
Useful at imaging renal vein and IVC tumour
thrombus
Presence of enhancement in the thrombus is able to distinguish between bland and tumour
thrombus
CASE REPORT
A 61 year old female patient presented to the Emergency Department with feeling unwell, pyrexia, nausea and headache. She gave a history of fever for the past three weeks with three episodes of rigors. She also gave a history of recent loss of appetite and some weight loss. She had no urinary problems.On examination she looked pale. A mass was palpable in the right lower quadrant and lumbar region. Liver and spleen were not palpable. There were no signs of peritonitis.Her pulse rate was 125/minute, BP 120/85 and temp 39.6 degree Centigrade. She had blood tests in the Emergency Department which revealed the following : Hb 12.0 g/dL, WCC 11.6 × 10(9)/litre and Platelets 237 × 10(9)/litre. Electrolytes and urea were as follows: Na 133 mmol/litre, K+ 4.2 mmol/litre, Urea 5.1 mmol/litre and Creatinine 78 micromol/litre. Chest X ray did not reveal any abnormality.The patient had a CT which showed mass in the right Kidney.
DIFERENTIAL DIAGNOSIS
Renal adenoma
Renal oncocytoma
Angiomyolipoma
RENAL ONCOCYTOMA
5% of resected primary adult
epithelial renal neoplasms
6th to 7th decades with a peak incidence
at 55 years of age
Up to three quarters of patients are asymptomatic
Large massPseudocapsule,
necrosis is usually absent
sharp central stellate scar
The only reliable feature is evidence of
metastasis or aggressive infiltration
small tumours may enhance
homogeneously, but usually enhancement is heterogenous and the mass is larger
tumour thrombus is absent
Angiography: spoke wheel pattern, during
the capillary phase the tumour demonstrates a
homogenous blush, lu acent avascular rim may be seen
due to the compressed pseudocapsule
ANGIOMYOLIPOMA
composed of vascular, smooth muscle and fat
elements
typically identified in adults (mean age of
presentation 43 years)F:M of 4:1
The remaining 20% are seen in association with phakomatoses,
the vast majority in the setting of tuberous
sclerosis
Retroperitoneal haemorrhage;
Wunderlich syndrome
palpable mass, flank pain, urinary tract
infections, haematuria, renal failure, hypertension
cornerstone of diagnosis on all modalities is the demonstration of macroscopic fat
in the setting of haemorrhage, or when
lesions contain little fat, appearances may
be difficult to distinguish
Most lesions involve the cortex and demonstrate
macroscopic fat (< - 20HU)
A proportion of angiomyolipomas are
fat-poor. This is especially the case in
the setting of tuberous sclerosis
Calcification is rare.
MRI: at saturated techniques
demonstrate high signal on non-fat
saturated sequences, and loss of signal
following fat saturation
india ink artifact at the interface between fat
and non-fat components
DSA - angiographyAngiomyolipomas are hypervascular
lesions demonstrating often characteristic features:
micro or macro aneurysms sharply marginateddense early arterial networklate whorled appearance
RENAL ADENOMA
>3 cm in patients of 50-70 years of age
Male predilection
CRR potential It´s benign if it´s >2cm
You can´t diferentiate it
from RRC