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Parts
apex of the bladder
fundus of the bladder
body of the bladder
neck of the bladder
Position of urinary bladder & its lymph drainage
Arterial supply & innervation
Arterial supply (male)
-. superior vesical
arteries
anterosuperior parts
of the bladder
-. inferior vesical
arteries fundus
and neck of the
bladder
-. vaginal arteries =
the inferior vesical
arteries and send
small branches to
posteroinferior parts
of the bladder
Proximal male urethra
muscular tube; conveys urine from the internal urethral
orifice of the urinary bladder to the external urethral
orifice
Arterial supply
prostatic branches of the inferior vesical and middle rectal
arteries
Venous & lymphatic drainage
prostatic venous plexus
internal iliac lymph nodes (mainly), external iliac lymph nodes
(few)
Innervations
derived from the prostatic plexus (mixed sympathetic,
parasympathetic, and visceral afferent fibers); arising as organ-
specific extensions of the inferior hypogastric plexus
Distal male urethra
The intermediate (membranous) part of the urethra
surrounded by the external urethral sphincter
It then penetrates the perineal membrane, ending as the urethra
enters the bulb of the penis
Posterolateral to this part of the urethra are the small
bulbourethral glands
The spongy urethra
it is expanded in the bulb of the penis to form the intrabulbar
fossa and in the glans of the penis to form the navicular fossa
many minute openings of the ducts of mucus-secreting urethral
glands
Arterial supply
from branches of the dorsal artery of the penis
Venous & lymphatic drainage
accompany the arteries and have similar names
Lymphatic vessels from the intermediate part of the urethra drain
mainly into the internal iliac lymph nodes; the spongy urethra pass to
the deep inguinal lymph nodes
Innervations
autonomic (efferent) innervation via the prostatic nerve plexus, arising
from the inferior hypogastric plexus
sympathetic innervation is from the lumbar spinal cord levels via the
lumbar splanchnic nerves, and the parasympathetic innervation is from
the sacral levels via the pelvic splanchnic nerves
dorsal nerve of the penis, a branch of the pudendal nerve, provides
somatic innervation of the spongy part of the urethra
Scrotum
cutaneous fibromuscular sac for the testes and associated
structures
Arterial supply
Anterior scrotal arteries; posterior scrotal arteries
Venous & lymphatic drainage
scrotal veins
superficial inguinal lymph nodes
Innervation
Anterior lumbar plexus: anterior scrotal nerves, derived from the
ilioinguinal nerve, and the genital branch of the genitofemoral nerve
Posterior sacral plexus: posterior scrotal nerves, branches of the
superficial perineal branches of the pudendal nerve, and the perineal
branch of the posterior femoral cutaneous nerve
Penis
male copulatory organ and, by conveying the urethra, provides
the common outlet for urine and semen
consists of a root, body, and glans
Arterial supply
Dorsal arteries of the penis; Deep arteries of the penis; Arteries of the
bulb of the penis
Venous & lymphatic drainage
deep dorsal vein of the penis; superficial dorsal vein
Lymph from the skin of the penis drains initially to the superficial
inguinal lymph nodes; glans & spongy urethra drain to the deep
inguinal and external iliac nodes; from the cavernous bodies and
proximal spongy urethra drain to the internal iliac nodes
Innervation
of penis
Female urethra
approximately 4 cm long and 6 mm in diameter; passes
anteroinferiorly from the internal urethral orifice of the
urinary bladder
The urethra passes with the vagina through the pelvic
diaphragm, external urethral sphincter, and perineal
membrane
Urethral glands are present, particularly in the superior
part of the urethra
One group of glands on each side, the paraurethral
glands, are homologues to the prostate
Arterial supply
internal pudendal and vaginal arteries
Venous & lymphatic drainage
veins follow the arteries and have similar names
sacral and internal iliac lymph nodes (mainly); inguinal lymph
nodes (few)
Innervations
vesical (nerve) plexus and the pudendal nerve
Female external genitalia
Arterial supply (vulva)
internal pudendal artery supplies most of the skin, external
genitalia, and perineal muscles. The labial arteries are branches
of the internal pudendal artery, as are those of the clitoris
Venous & lymphatic drainage (vulva)
labial veins are tributaries of the internal pudendal veins
superficial inguinal lymph nodes
Innervation (vulva)
Anterior lumbar plexus: the anterior labial nerves, derived from the
ilioinguinal nerve, and the genital branch of the genitofemoral nerve
Posterior derivatives of the sacral plexus: the perineal branch of
the posterior cutaneous nerve of the thigh laterally and the pudendal
nerve centrally
posterior labial nerves labia
deep and muscular branches of the perineal nerve supply the orifice
of the vagina and superficial perineal muscles
dorsal nerve of the clitoris supplies deep perineal muscles and
sensation to the clitoris
The bulb of the vestibule and erectile bodies of the clitoris receive
parasympathetic fibers via cavernous nerves from the uterovaginal
nerve plexus
LO 1.2
Menjelaskan histologi traktus urinarius
Kidney
Nephrons The smallest fungsional units of kidney
Blood circulation (Kidney)
Renal Corpuscles & Blood Filtration
Glomerular filtration barrier
Components:
-. macula densa
-. juxtaglomerular
granular (JG) cells
-. lacis cells
Collecting tubules & ducts
Ureter
Components of urothelium:
-. an intermediate region
containing from one to several
layers of more columnar cells
Etiology
follows infection of the throat or skin by certain "nephritogenic" strains
of group A β-hemolytic streptococci
Epidemiology
commonly follows streptococcal pharyngitis during cold weather
months and streptococcal skin infections or pyoderma during warm
weather months
epidemics of nephritis have been described in association with both
throat (serotype 12) and skin (serotype 49) infections
Pathology
-. all glomeruli appear enlarged and relatively bloodless and show diffuse mesangial
cell proliferation with an increase in mesangial matrix
-. Polymorphonuclear leukocytes are common in glomeruli during the early stage of
the disease
Pathogenesis
Mediated by immune complexes
Clinical course
a young child abruptly develops malaise, fever, nausea, oliguria, and
hematuria 1 to 2 weeks after recovery from a sore throat / 3-6 wk
after a streptococcal pyoderma
red cell casts in the urine, mild proteinuria (usually less than 1
gm/day), periorbital edema, and mild to moderate hypertension
acute phase generally resolves within 6-8 wk
urinary protein excretion and hypertension usually normalize by 4-6
wk after onset
persistent microscopic hematuria may persist for 1-2 yr after the initial
presentation
Clinical manifestations
various degrees of edema, hypertension, and oliguria
Patients may develop encephalopathy and/or heart failure
owing to hypertension or hypervolemia
malaise, lethargy, abdominal or flank pain, and fever are
common
Diagnosis
Urinalysis red blood cells (RBCs), frequently in association with RBC
casts, proteinuria, and polymorphonuclear leukocytes
mild normochromic anemia
low-grade hemolysis
The serum C3 level is usually reduced in the acute phase
A positive throat culture
antistreptolysin O titer is commonly elevated after a pharyngeal
infection
to document cutaneous streptococcal infection is the
deoxyribonuclease (DNase) B antigen
renal biopsy is considered when hematuria and proteinuria, diminished
renal function, and/or a low C3 level persist more than 2 mo after
onset
Complications
Hypertension is seen in 60% of patients and may be associated
with hypertensive encephalopathy in 10% of cases
heart failure
Hyperkalemia
Hyperphosphatemia
Hypocalcemia
Acidosis
Seizures
Uremia
Prevention
Early systemic antibiotic therapy for streptococcal throat and
skin infections does not eliminate the risk of glomerulonephritis
Family members of patients with acute glomerulonephritis should
be cultured for group A β-hemolytic streptococci and treated if
culture positive
Treatment
a 10-day course of systemic antibiotic therapy with penicillin is
recommended to limit the spread of the nephritogenic organisms
Hypertension treatment
Prognosis
Complete recovery occurs in more than 95% of children
Mortality in the acute stage can be avoided by appropriate
management of acute renal failure, cardiac failure, and
hypertension
Infrequently, the acute phase may be severe and lead to
glomerular hyalinization and chronic renal insufficiency
Recurrences are extremely rare
LO 2.2 Nephrotic syndrome
Certain glomerular diseases virtually always produce the
nephrotic syndrome
Pathophysiology
Manifestations
Massive proteinuria, with the daily loss of 3.5 gm or more of protein
(less in children)
Hypoalbuminemia, with plasma albumin levels less than 3 gm/dL
Generalized edema
Hyperlipidemia and lipiduria
Causes
Idiopathic nephrotic syndrome
Diagnosis
urinalysis reveals 3+ or 4+ proteinuria
Microscopic hematuria (20%)
A spot urine protein:creatinine ratio exceeds 2.0
urinary protein > 40 mg/m2/hr
serum albumin level is <2.5 g/dL
serum cholesterol, triglyceride levels are elevated
Treatment
Prednisolone 60 mg/m2/day (maximum daily dose, 80 mg) a
single daily dose for 4-6 consecutive wk prednisone dose should be
tapered to 40 mg/m2/day given every other day as a single daily dose
for at least 4 wk
Secondary nephrotic syndrome
Congenital nephritic syndrome
nephrotic syndrome manifesting at birth or within the
first 3 mo of life
Other genetic causes
LO 2.3 Acute renal failure
rapid decline in glomerular filtration rate (GFR) over hours
to days
usually asymptomatic and diagnosed when biochemical
monitoring of hospitalized patients reveals a new increase in
blood urea and serum creatinine concentrations
Categories
that cause renal hypoperfusion, resulting in decreased function without
frank parenchymal damage (prerenal ARF, or azotemia) (~55%)
diseases that directly involve the renal parenchyma (intrinsic ARF)
(~40%)
diseases associated with urinary tract obstruction (postrenal ARF)
(~5%)
Prerenal ARF (Prerenal Azotemia)
Etiology
Pathophysiology
Hypovolemia leads to a fall in mean systemic arterial pressure
detected as reduced stretch by arterial (e.g., carotid sinus) and
cardiac baroreceptors
activation of the sympathetic nervous system and renin-angiotensin-
aldosterone system
salt loss through sweat glands is inhibited, and thirst and salt appetite
are stimulated. Renal salt and water retention also occur
In response to the reduction in perfusion pressure, stretch receptors in
afferent arterioles trigger afferent arteriolar vasodilatation through a
local myogenic reflex
constriction of efferent arterioles
GFR is preserved more severe hypovolemia AFR
Intrinsic ARF
Etiology
Postrenal ARF
Etiology
Clinical assesment
Prerenal ARF
Intrinsic ARF
Complication
Expansion of extracellular fluid volume hypoosmolality and
hyponatremia lead to neurologic abnormalities, including
seizures
Hyperkalemia
metabolic acidosis
Hyperphosphatemia
Anemia
uremic syndrome
A vigorous diuresis can occur during the recovery phase of ARF
Prevention
Adjusting drug dosage (estimate the GFR using the Cockcroft-
Gault formula)
Etiology
result of congenital, acquired, inherited, or metabolic renal disease
children younger than 5 yr is most commonly a result of congenital
abnormalities such as renal hypoplasia, dysplasia, and/or obstructive
uropathy
After 5 yr of age, acquired diseases (various forms of
glomerulonephritis) and inherited disorders (familial juvenile
nephronophthisis, Alport syndrome) predominate
related to metabolic disorders (cystinosis, hyperoxaluria) and certain
inherited disorders (polycystic kidney disease) may present throughout
the childhood years
Classification
Mild chronic renal insufficiency: GFR 50-75 mL/min/l.73 m2
Moderate chronic renal insufficiency: GFR 25-50 mL/min/l.73
m2
Chronic renal failure (CRF): GFR 10-25 mL/min/l.73 m2
End stage renal disease (ESRD): GFR < 10 mL/min/l.73 m2
Clinical Manifestations
Anemia in patients with CRF is primarily the result of inadequate
erythropoietin production by the failing kidneys and usually
becomes manifest at a GFR less than 35 mL/min/1.73 m2
The term renal osteodystrophy is used to indicate a spectrum of
bone disorders seen in patients with CRF.
The most common condition seen in children is high-turnover
bone disease caused by secondary hyperparathyroidism
Acidosis maintain the serum bicarbonate level above 22
mEq/L sodium bicarbonate tablets (650 mg equals 8 mEq of
base)
Children with high blood pressure, edema, or heart failure
sodium restriction and diuretic therapy
Hyperkalemia restriction of dietary potassium intake,
administration of oral alkalinizing agents, and/or treatment with
Kayexalate.
Nutritions
Dietary phosphorus, potassium, and sodium should be restricted
according to the individual patient's laboratory studies and fluid
balance.
Protein intake should be 2.5 g/kg/24 hr and should consist of
proteins of high biologic value that are metabolized primarily
to usable amino acids rather than to nitrogenous wastes. The
proteins of highest biologic value are those of eggs and milk,
followed by meat, fish, and fowl.
Tatalaksana
replacing absent/ diminished renal functions, which
progressively increase in parallel with the progressive loss of
GFR,
slowing the progression of renal dysfunction
Daftar pustaka
Dalley, Arthur F. Keith L Moore. Clinically Oriented
Anatomy. 5th edition. Lippincott Williams & Wilcins; 2006
Nelson Textbook of Pediatric, 19th edition
Sherwood,Lauralee. Fisiologi Manusia dari Sel ke Sistem.
Cetakan pertama edisi 2. Jakarta: EGC; 2001
Fauci. Braunwald. Dkk. Harrison’s Principles of Internal
Medicine. 17th edition. United State: The McGraw-Hills;
2008
Guyton and Hall medical physiology