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Lumbar mass
Anatomy of lumbar area
lumbar
colon
kidney
Adrenal
Retroperitoneum
Dullness in renal mass
Resonant normally and in case of splenic
or colonic masses
pathology
Colonic mass
• pericolic abscess
• carcinoma
Pericolic abscess
• complication of diverticulosis / IBD/amoebic
colitis
• pain , fever , leucocytosis, tender illdefined
fluctuant mass
• Hinchey classification
Stage I: pericolic or mesenteric abscess
Stage II: walled-off pelvic abscess
Stage III: generalized purulent peritonitis
Stage IV: generalized fecal peritonitis
• USG ,CT, MRI, barium enema is contraindicated
• IV antibiotics , USG/CT guided aspiration , colectomy
Ca colon
unexplained anemia is the common
presentation
Altered bowel habits , obstruction ,
perfotation, bleeding
 hard, nontender, fixed mass
Aetiology
1. DIET -Red meat, saturated fat and cholesterol
2.Alcohol and smoking
3.Radiation
4. Post-cholecystectomy and ileal resection and
ureterocolostomy status
5.Genetic causes
Familial Adenomatous polyposis coli.
Gardner's syndrome and Turcot’s syndrome.
Peutz jeger’s syndrome and Juvenile polyposis
syndrome.
HNPCC , Lynch syndrome1, Lynch syndrome 2
Aspirin and other NSAIDs, calcium are protective
against large bowel cancers
Types
1.Polypoidal
2.Ulcerative,
3.Annular,
4.proliferative
Investigations-stool for occult blood,
Barium meal follow through-irregular filling defect
Colonoscopy & Biopsy, CECT
Treatement - Right hemicolectomy, left hemicolectomy
chemotherapy (FOLFOX)
Retroperitoneal sarcoma
• liposarcoma is commonest sarcoma
• present as asymptomatic mass , obstruction
of bowel , ureter , vessels
• CECT , MRI
• wide local excision , multivisceral resection
• chemoradiation
Adrenal tumours
Adrenal cortical tumours
o Mostly benign (1%malignant)
o functioning or non-functioning tumours
o functioning tumours secrete sex hormones ,
mineralocorticoid , glucocorticoid
o non-functioning tumours commonly present as
incidentalomas
o Diagnosis by hormone assay, USG, CT
o adrenalectomy for benign adenomas
o Radical adrenalectomy+chemotherapy
Adrenal medullary tumours
neuroblastoma
• Commonest childhood tumour.
• It is a tumour of adrenal medulla.
• An aggressive malignant tumour in childhood
usually below the age of 5 years.
• asymptomatic mass , liver secondaries , orbital
secondaries , dancing eye syndrome ,
opsomyoclonus
• USG, CT, MRI, MIBG scan , urinary VMA
• adrenalectomy , debulking , chemotherapy
PHAEOCHROMOCYTOMA
• adrenal medullary tumour
• it is a norepinephrine secreting tumour
• benign or malignant
• headache , persistant or paroxysmal
hypertension , sympathetic overactivity
• may be associated with MEN-2 syndrome
• serum/ urinary
metanephrines/normetanephrines USG, CT, MRI,
MIBG scan
• surgical resection
Renal masses
• Cystic diseases of kidney
• hydronephrosis
• inflammatory mass
• Perinephric abscess
• renal tumours
Renal cysts
• simple cysts
• polycystic kidney disease
• medullary sponge kidney
• Multicystic kidney disease
• acquired cysts(hydatid cysts, dialysis)
• Asymptomatic, pain, hypertension , CRF
• aspiration , deroofing, marsupialisation,
hemodialysis, nephrectomy & transplantion
Hydronephrosis
• Due to obstruction of urine outflow
Hydronephrosis
Extramural
1.Aberrant renal vessels
2. carcinoma
3. Retroperitoneal fibrosis.
4. Retrocaval ureter
5.BPH
intramural
1.Congenital PUJ obstruction.
2. Ureterocele.
3. Neoplasm of ureter.
4. Narrow ureteric orifice.
5. Stricture ureter( stone,
pelvicsurgeries or tuberculosis )
Intraluminal
1.Stone
2. Sloughed papilla in papillary
necrosis
3.Phimosis
• Transient or persistant mass(dietl’s crisis) ,
renal failure
• IVU , USG , CT
• treatment according to the cause
Trauma
• Perirenal hematoma
Inflammatory
• Tuberculosis
• Pyonephrosis
• Perinephric abscess
• Renal Carbuncle
• USG , CT
• antibiotics , aspiration , drainage ,
nephrectomy
Neoplasms
Benign
• papillary adenomas
• medullary fibroma
• lipoma
Malignant
• Renal cell carcinoma
• wilms tumour
Wilms tumour
• common in first 4 years of life.
• arises from embryonic tissue containing epithelial
and connective tissue elements.
• bilateral in 5% cases.
• mass , fever, pain, hypertension , hematuria ,
congenital anomalies
• USG, CT, MRI,IVU
• nephroureterectomy + chemotherapy +
radiotherapy
Renal cell carcinoma
• Hypernephroma, Grawitz tumour
• It is an adenocarcinoma arising from renal
tubular cells
• More common in males; more common in 5th-
6th decade of life.
• von Hippel-Lindau disease , Birt-Hogg-Dube’
syndrome , tuberous sclerosis
• Diet high in animal fat
• asbestos, lead, cadmium
• Tobacco & Cigarette smoking
• long-term dialysis
• Analgesic nephropathy
• Mass , hematuria , clot colic ,varicocele,
secondaries , fever , polycythemia, stauffer
syndrome
• USG , CT , MRI ,IVU
• Radical nephrectomy / chemotherapy

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Lumbar mass

  • 2.
  • 3.
  • 4. Anatomy of lumbar area lumbar colon kidney Adrenal Retroperitoneum
  • 5.
  • 6.
  • 7.
  • 8.
  • 9. Dullness in renal mass Resonant normally and in case of splenic or colonic masses
  • 11. Colonic mass • pericolic abscess • carcinoma
  • 12. Pericolic abscess • complication of diverticulosis / IBD/amoebic colitis • pain , fever , leucocytosis, tender illdefined fluctuant mass • Hinchey classification Stage I: pericolic or mesenteric abscess Stage II: walled-off pelvic abscess Stage III: generalized purulent peritonitis Stage IV: generalized fecal peritonitis • USG ,CT, MRI, barium enema is contraindicated • IV antibiotics , USG/CT guided aspiration , colectomy
  • 13. Ca colon unexplained anemia is the common presentation Altered bowel habits , obstruction , perfotation, bleeding  hard, nontender, fixed mass
  • 14.
  • 15. Aetiology 1. DIET -Red meat, saturated fat and cholesterol 2.Alcohol and smoking 3.Radiation 4. Post-cholecystectomy and ileal resection and ureterocolostomy status 5.Genetic causes Familial Adenomatous polyposis coli. Gardner's syndrome and Turcot’s syndrome. Peutz jeger’s syndrome and Juvenile polyposis syndrome. HNPCC , Lynch syndrome1, Lynch syndrome 2 Aspirin and other NSAIDs, calcium are protective against large bowel cancers
  • 16. Types 1.Polypoidal 2.Ulcerative, 3.Annular, 4.proliferative Investigations-stool for occult blood, Barium meal follow through-irregular filling defect Colonoscopy & Biopsy, CECT Treatement - Right hemicolectomy, left hemicolectomy chemotherapy (FOLFOX)
  • 17. Retroperitoneal sarcoma • liposarcoma is commonest sarcoma • present as asymptomatic mass , obstruction of bowel , ureter , vessels • CECT , MRI • wide local excision , multivisceral resection • chemoradiation
  • 18.
  • 19. Adrenal tumours Adrenal cortical tumours o Mostly benign (1%malignant) o functioning or non-functioning tumours o functioning tumours secrete sex hormones , mineralocorticoid , glucocorticoid o non-functioning tumours commonly present as incidentalomas o Diagnosis by hormone assay, USG, CT o adrenalectomy for benign adenomas o Radical adrenalectomy+chemotherapy
  • 20. Adrenal medullary tumours neuroblastoma • Commonest childhood tumour. • It is a tumour of adrenal medulla. • An aggressive malignant tumour in childhood usually below the age of 5 years. • asymptomatic mass , liver secondaries , orbital secondaries , dancing eye syndrome , opsomyoclonus • USG, CT, MRI, MIBG scan , urinary VMA • adrenalectomy , debulking , chemotherapy
  • 21. PHAEOCHROMOCYTOMA • adrenal medullary tumour • it is a norepinephrine secreting tumour • benign or malignant • headache , persistant or paroxysmal hypertension , sympathetic overactivity • may be associated with MEN-2 syndrome • serum/ urinary metanephrines/normetanephrines USG, CT, MRI, MIBG scan • surgical resection
  • 22. Renal masses • Cystic diseases of kidney • hydronephrosis • inflammatory mass • Perinephric abscess • renal tumours
  • 23. Renal cysts • simple cysts • polycystic kidney disease • medullary sponge kidney • Multicystic kidney disease • acquired cysts(hydatid cysts, dialysis) • Asymptomatic, pain, hypertension , CRF • aspiration , deroofing, marsupialisation, hemodialysis, nephrectomy & transplantion
  • 24.
  • 25. Hydronephrosis • Due to obstruction of urine outflow Hydronephrosis Extramural 1.Aberrant renal vessels 2. carcinoma 3. Retroperitoneal fibrosis. 4. Retrocaval ureter 5.BPH intramural 1.Congenital PUJ obstruction. 2. Ureterocele. 3. Neoplasm of ureter. 4. Narrow ureteric orifice. 5. Stricture ureter( stone, pelvicsurgeries or tuberculosis ) Intraluminal 1.Stone 2. Sloughed papilla in papillary necrosis 3.Phimosis
  • 26.
  • 27. • Transient or persistant mass(dietl’s crisis) , renal failure • IVU , USG , CT • treatment according to the cause
  • 29. Inflammatory • Tuberculosis • Pyonephrosis • Perinephric abscess • Renal Carbuncle • USG , CT • antibiotics , aspiration , drainage , nephrectomy
  • 30. Neoplasms Benign • papillary adenomas • medullary fibroma • lipoma Malignant • Renal cell carcinoma • wilms tumour
  • 31. Wilms tumour • common in first 4 years of life. • arises from embryonic tissue containing epithelial and connective tissue elements. • bilateral in 5% cases. • mass , fever, pain, hypertension , hematuria , congenital anomalies • USG, CT, MRI,IVU • nephroureterectomy + chemotherapy + radiotherapy
  • 32. Renal cell carcinoma • Hypernephroma, Grawitz tumour • It is an adenocarcinoma arising from renal tubular cells • More common in males; more common in 5th- 6th decade of life.
  • 33. • von Hippel-Lindau disease , Birt-Hogg-Dube’ syndrome , tuberous sclerosis • Diet high in animal fat • asbestos, lead, cadmium • Tobacco & Cigarette smoking • long-term dialysis • Analgesic nephropathy
  • 34. • Mass , hematuria , clot colic ,varicocele, secondaries , fever , polycythemia, stauffer syndrome • USG , CT , MRI ,IVU • Radical nephrectomy / chemotherapy