Renal and urinary tract masses: Pathology review

Last updated: January 17, 2022

Renal and urinary tract masses: Pathology review

Metabolism HYMS year 3

Metabolism HYMS year 3

Anatomy of the abdominal viscera: Kidneys, ureters and suprarenal glands
Anatomy of the urinary organs of the pelvis
Anatomy of the female urogenital triangle
Anatomy of the perineum
Anatomy clinical correlates: Male pelvis and perineum
Anatomy clinical correlates: Female pelvis and perineum
Development of the renal system
Ureter, bladder and urethra histology
Kidney histology
Renal system anatomy and physiology
Hydration
Body fluid compartments
Movement of water between body compartments
Renal clearance
Glomerular filtration
TF/Px ratio and TF/Pinulin
Measuring renal plasma flow and renal blood flow
Regulation of renal blood flow
Tubular reabsorption and secretion
Tubular secretion of PAH
Tubular reabsorption of glucose
Urea recycling
Tubular reabsorption and secretion of weak acids and bases
Proximal convoluted tubule
Loop of Henle
Distal convoluted tubule
Renin-angiotensin-aldosterone system
Sodium homeostasis
Potassium homeostasis
Phosphate, calcium and magnesium homeostasis
Osmoregulation
Antidiuretic hormone
Kidney countercurrent multiplication
Free water clearance
Vitamin D
Erythropoietin
Physiologic pH and buffers
Buffering and Henderson-Hasselbalch equation
The role of the kidney in acid-base balance
Acid-base map and compensatory mechanisms
Respiratory acidosis
Metabolic acidosis
Plasma anion gap
Respiratory alkalosis
Metabolic alkalosis
Renal agenesis
Horseshoe kidney
Potter sequence
Hyperphosphatemia
Hypophosphatemia
Hypernatremia
Hyponatremia
Hypermagnesemia
Hypomagnesemia
Hyperkalemia
Hypokalemia
Hypercalcemia
Hypocalcemia
Renal tubular acidosis
Minimal change disease
Diabetic nephropathy
Focal segmental glomerulosclerosis (NORD)
Amyloidosis
Membranous nephropathy
Lupus nephritis
Poststreptococcal glomerulonephritis
Rapidly progressive glomerulonephritis
IgA nephropathy (NORD)
Alport syndrome
Kidney stones
Hydronephrosis
Acute pyelonephritis
Chronic pyelonephritis
Prerenal azotemia
Renal azotemia
Acute tubular necrosis
Postrenal azotemia
Renal papillary necrosis
Renal cortical necrosis
Chronic kidney disease
Polycystic kidney disease
Multicystic dysplastic kidney
Medullary cystic kidney disease
Medullary sponge kidney
Renal artery stenosis
Renal cell carcinoma
Angiomyolipoma
Nephroblastoma (Wilms tumor)
WAGR syndrome
Beckwith-Wiedemann syndrome
Posterior urethral valves
Hypospadias and epispadias
Vesicoureteral reflux
Bladder exstrophy
Urinary incontinence
Neurogenic bladder
Lower urinary tract infection
Transitional cell carcinoma
Non-urothelial bladder cancers
Congenital renal disorders: Pathology review
Renal tubular defects: Pathology review
Renal tubular acidosis: Pathology review
Acid-base disturbances: Pathology review
Electrolyte disturbances: Pathology review
Renal failure: Pathology review
Nephrotic syndromes: Pathology review
Nephritic syndromes: Pathology review
Urinary incontinence: Pathology review
Urinary tract infections: Pathology review
Kidney stones: Pathology review
Renal and urinary tract masses: Pathology review
Osmotic diuretics
Carbonic anhydrase inhibitors
Loop diuretics
Thiazide and thiazide-like diuretics
Potassium sparing diuretics
ACE inhibitors, ARBs and direct renin inhibitors
Endocrine system anatomy and physiology
Hunger and satiety
Insulin
Glucagon
Somatostatin
Diabetes mellitus
Diabetic retinopathy
Pancreatic neuroendocrine neoplasms
Parathyroid disorders and calcium imbalance: Pathology review
Diabetes insipidus and SIADH: Pathology review
Hyperthyroidism medications
Hypothyroidism medications
Insulins
Hypoglycemics: Insulin secretagogues
Miscellaneous hypoglycemics
Diabetes mellitus: Pathology review
Prostatitis
Prostate disorders and cancer: Pathology review
Prostate cancer
Prostate gland histology
Androgens and antiandrogens
PDE5 inhibitors
Adrenergic antagonists: Alpha blockers
Hyperthyroidism
Graves disease
Thyroid eye disease (NORD)
Toxic multinodular goiter
Thyroid storm
Euthyroid sick syndrome
Thyroid hormones
Hashimoto thyroiditis
Subacute granulomatous thyroiditis
Hypothyroidism
Thyroglossal duct cyst
Riedel thyroiditis
Thyroid cancer
Congenital adrenal hyperplasia
Primary adrenal insufficiency
Waterhouse-Friderichsen syndrome
Hyperaldosteronism
Adrenal cortical carcinoma
Cushing syndrome
Conn syndrome
Hyperparathyroidism
Hypoparathyroidism
Hyperpituitarism
Pituitary adenoma
Hyperprolactinemia
Prolactinoma
Gigantism
Acromegaly
Hypopituitarism
Pituitary apoplexy
Sheehan syndrome
Hypoprolactinemia
Constitutional growth delay
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Precocious puberty
Delayed puberty
Premature ovarian failure
Polycystic ovary syndrome
Androgen insensitivity syndrome
Kallmann syndrome
5-alpha-reductase deficiency
Autoimmune polyglandular syndrome type 1 (NORD)
Multiple endocrine neoplasia
Zollinger-Ellison syndrome
Carcinoid syndrome
Pheochromocytoma
Neuroblastoma
Opsoclonus myoclonus syndrome (NORD)
Adrenal insufficiency: Pathology review
Adrenal masses: Pathology review
Hyperthyroidism: Pathology review
Hypothyroidism: Pathology review
Thyroid nodules and thyroid cancer: Pathology review
Cushing syndrome and Cushing disease: Pathology review
Pituitary tumors: Pathology review
Hypopituitarism: Pathology review
Multiple endocrine neoplasia: Pathology review
Adrenal hormone synthesis inhibitors
Mineralocorticoids and mineralocorticoid antagonists
Synthesis of adrenocortical hormones
Cortisol
Testosterone
Estrogen and progesterone
Parathyroid hormone
Calcitonin
Adrenocorticotropic hormone
Growth hormone and somatostatin
Oxytocin and prolactin
Pituitary gland histology
Pancreas histology
Thyroid and parathyroid gland histology
Adrenal gland histology
Iron deficiency anemia
Alpha-thalassemia
Beta-thalassemia
Sideroblastic anemia
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Anemia of chronic disease
Lead poisoning
Hemolytic disease of the newborn
Autoimmune hemolytic anemia
Pyruvate kinase deficiency
Paroxysmal nocturnal hemoglobinuria
Hereditary spherocytosis
Sickle cell disease (NORD)
Fanconi anemia
Megaloblastic anemia
Folate (Vitamin B9) deficiency
Aplastic anemia
Vitamin B12 deficiency
Diamond-Blackfan anemia
Acute intermittent porphyria
Porphyria cutanea tarda
Hemophilia
Vitamin K deficiency
Hemolytic-uremic syndrome
Bernard-Soulier syndrome
Glanzmann's thrombasthenia
Immune thrombocytopenia
Thrombotic thrombocytopenic purpura
Von Willebrand disease
Disseminated intravascular coagulation
Heparin-induced thrombocytopenia
Factor V Leiden
Protein C deficiency
Protein S deficiency
Antiphospholipid syndrome
Antithrombin III deficiency
Hodgkin lymphoma
Non-Hodgkin lymphoma
Chronic leukemia
Acute leukemia
Myelodysplastic syndromes
Polycythemia vera (NORD)
Myelofibrosis (NORD)
Essential thrombocythemia (NORD)
Leukemoid reaction
Langerhans cell histiocytosis
Multiple myeloma
Monoclonal gammopathy of undetermined significance
Waldenstrom macroglobulinemia
Mastocytosis (NORD)
Microcytic anemia: Pathology review
Non-hemolytic normocytic anemia: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Macrocytic anemia: Pathology review
Heme synthesis disorders: Pathology review
Coagulation disorders: Pathology review
Platelet disorders: Pathology review
Mixed platelet and coagulation disorders: Pathology review
Thrombosis syndromes (hypercoagulability): Pathology review
Lymphomas: Pathology review
Leukemias: Pathology review
Plasma cell disorders: Pathology review
Myeloproliferative disorders: Pathology review
Anticoagulants: Heparin
Anticoagulants: Warfarin
Anticoagulants: Direct factor inhibitors
Antiplatelet medications
Thrombolytics
Hematopoietic medications
Ribonucleotide reductase inhibitors
Topoisomerase inhibitors
Platinum containing medications
Anti-tumor antibiotics
Microtubule inhibitors
DNA alkylating medications
Monoclonal antibodies
Antimetabolites for cancer treatment
Anatomy of the thyroid and parathyroid glands
Pharyngeal arches, pouches, and clefts
Blood histology
Blood components
Blood groups and transfusions
Platelet plug formation (primary hemostasis)
Coagulation (secondary hemostasis)
Role of Vitamin K in coagulation
Clot retraction and fibrinolysis
Anatomy clinical correlates: Other abdominal organs
Anatomy of the male urogenital triangle
Membranoproliferative glomerulonephritis
von Hippel-Lindau disease
Klinefelter syndrome
Turner syndrome
Benign prostatic hyperplasia
Cryptorchidism
Varicocele
Orchitis
Testicular cancer
Epididymitis
Testicular torsion
Priapism
Penile cancer
Urethritis
Proteus mirabilis
Testicular tumors: Pathology review
Kidney stones: Clinical
Renal cysts and cancer: Clinical
Testicular and scrotal conditions: Pathology review
Anatomy clinical correlates: Inguinal region
Blood products and transfusion: Clinical
Venous thromboembolism: Clinical
Hypernatremia: Clinical
Hyponatremia: Clinical
Hyperkalemia: Clinical
Hypokalemia: Clinical
Metabolic and respiratory acidosis: Clinical
Metabolic and respiratory alkalosis: Clinical
Acute kidney injury: Clinical
Transplant rejection
Graft-versus-host disease
Cytomegalovirus infection after transplant (NORD)
Post-transplant lymphoproliferative disorders (NORD)
Rhabdomyolysis

Transcript

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In the Emergency Department, two people came in. One of them is 68 years old Randy who has left flank pain and gross hematuria. On the physical examination, there’s also a palpable mass in the left abdomen. Randy also has a history of heavy smoking for the past 40 years. The other person is 54 year old Uriah who came in because of painless hematuria. A while ago, Uriah took cyclophosphamide for a condition he had called Hodgkin’s disease. Both individuals had an ultrasound done, which showed a mass in Randy’s left kidney and a mass in Uriah’s bladder.

Okay, Randy has a mass in his left kidney, while Uriah has a mass in his bladder. Let’s first talk about renal masses, which can develop in both adults and children. These masses may be either cysts or tumor. In turn, renal cysts can be either simple or complex, while tumors can be benign, like renal oncocytoma, or malignant, like renal cell carcinoma. Regarding masses of the urinary tract, the main concerns are transitional cell carcinoma and squamous carcinoma of the bladder.

Let’s look at them one by one. Simple cysts are very common and account for most of renal masses. They are typically small and occur in adults with otherwise healthy kidneys. On an abdominal ultrasound, they’re perfectly round and have a thin wall and are filled with fluid. This liquid is basically the produced by the kidney. The ultrafiltrate is the plasma without proteins that results after the filtration process, that happens in the glomeruli, specifically in Bowman’s capsule. This makes simple cysts anechoic on ultrasound, since the fluid does not produce an echo and thus appear black. Usually they’re asymptomatic and are discovered incidentally during an ultrasound or a CT-scan done for other reasons. On the other hand, complex cysts are larger than simple cysts. Additionally, on an ultrasound, they have thick, irregular walls and are multilocular- meaning they have septations within, that separate the cyst cavity into compartiments. Sometimes, complex cysts may even have a solid component within. Now, complex cysts are more likely to cause symptoms, like flank pain, for example. They also have a higher chance of becoming malignant and that’s why, for your tests, remember that complex cysts require additional follow up and even surgical removal.

Let’s now talk about renal oncocytoma, which is a benign tumor that usually appears in adults. It originates from the intercalated cells of the collecting ducts. Macroscopically, the tumor appears as a circumscribed mass with a central scar. Microscopically, unlike RCC, a renal oncocytoma has large eosinophilic cells without perinuclear clearing. Individuals can present with painless hematuria, flank pain and an abdominal mass. Most of these benign tumors are resected in order to rule out malignancies, like RCC.

Moving onto renal cell carcinoma or RCC, which is the most common renal malignancy. It usually appears in males between the ages of 50 to 70. Risk factors for RCC include smoking and obesity. It’s associated with mutations that cause gene deletions on chromosome 3. These mutations can be sporadic or inherited as a part of Von-Hippel-Lindau syndrome, which is characterized by the formation of cysts and tumors in different parts of the body, like the kidneys and pancreas.

Now, RCC originates from the proximal convoluted tubule’s epithelial cells. For your tests, remember that, the most common type of RCC is a clear cell carcinoma, where the cancerous cells are polygonal and filled with lipids and carbohydrates. They appear clear on microscopy, because the standard tissue fixation and staining techniques dissolve the lipids and glycogen, leaving clear empty spaces behind. Now, RCC can invade the renal vein and if it invades the renal vein on the left side, it can lead to a varicocele. This is because the venous drainage from the left testis travels through the left testicular vein and then through the left renal vein and finally, in the inferior vena cava. So, if RCC invades the left renal vein, then the venous drainage of the left testis is blocked, leading to a varicocele. Remember for your exams that this can never happen on the right side, because the venous drainage from the right testis goes directly into the inferior vena cava. Now that we got that covered, RCC can also invade the inferior vena cava via the renal veins and through hematogenous spread, can cause metastasis to the lungs and bones.

RCC can be asymptomatic, but it can also present with the classic triad of flank pain, hematuria and palpable masses. That’s because if the tumor is big enough, it will compress the surrounding tissues, leading to flank pain and a palpable mass. This compression can also damage the kidney, causing hematuria. In more advanced stages, weight loss can also be present. Now, RCC can also be associated with signs and symptoms of a paraneoplastic syndrome. First, the tumor can secrete erythropoietin and this will affect the bone marrow, making it produce more red blood cells in which case there will be polycythemia. In other cases, the tumor can also secrete a PTH-related protein, which acts just like Parathyroid hormone and cause the bones to release more calcium, leading to hypercalcemia. It can also produce ACTH, which causes the adrenal glands to overproduce cortisol and there will be signs of Cushing syndrome, like Moon facies, buffalo hump, and hypertension. Finally, it can also produce renin, which is normally produced by the kidneys. Renin further activated the renin-angiotensin-aldosterone system, leading to hypertension.

Key Takeaways

Renal and urinary tract masses are abnormal growths that can develop in the kidneys, ureters, bladder, and urethra. These masses may be either cysts or tumors. Renal cysts on ultrasounds appear to be tiny sacs filled with black fluid. Cysts can be either simple or complex when they have septations within. Renal tumors can be benign, like renal oncocytoma, or malignant, like renal cell carcinoma. Common urinary tract tumors include: Renal cell carcinoma: the most common type of renal cancer. It develops in the renal tubules and can metastasize to surrounding tissue. Transitional cell carcinoma: develops in the urothelial cells lining the urinary tract. Wilms' tumor: a rare type of kidney cancer typically affecting children.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Robbins and Cotran Pathologic Basis of Disease" Saunders (2015)
  4. "Fundamentals of Pathology" H.A. Sattar (2011)
  5. "Renal cell carcinoma" The Lancet (2009)
  6. "Gemcitabine and Cisplatin Versus Methotrexate, Vinblastine, Doxorubicin, and Cisplatin in Advanced or Metastatic Bladder Cancer: Results of a Large, Randomized, Multinational, Multicenter, Phase III Study" Journal of Clinical Oncology (2000)
  7. "Maintaining protein stability of ∆Np63 via USP 28 is required by squamous cancer cells" EMBO Molecular Medicine (2020)