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Embryology urogenital system

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  • 1. EMBRYOLOGYBY
    Dr. THAAER MOHAMMED DAHER ALSAAD
    SPECIALIST IN GENERAL SURGERY
    M.B.Ch.B. (MBBS) F.I.B.M.S. (PhD)
    SENIOR LECTURER
    ISM MSU
  • 2. Urogenital System
  • 3. Urogenital System
    Functionally the urogenital system can be divided into two entirely different components:
    The urinary system
    The genital system.
    • Embryologically and anatomically they are intimately interwoven.
    • 4. Both develop from a common mesodermal ridge (intermediate mesoderm) along the posterior wall of the abdominal cavity,
    • 5. Initially the excretory ducts of both systems enter a common cavity, the cloaca.
  • Urinary SystemKIDNEY SYSTEMS
    Three slightly overlapping kidney systems are formed in a cranial to caudal sequence during intrauterine life in humans:
    The pronephros, (rudimentary and nonfunctional).
    The mesonephros, (function for a short time during the early fetal period).
    The metanephros, (forms the permanent kidney)
  • 6. 21 days
    25 days
    Transverse sections through embryos at various stages of development
    showing formation of nephric tubules.
    Note formation of external and internal glomeruli and the open connection between the intraembryonic cavity and the nephric tubule.
  • 7. Pronephros
    At the beginning of the fourth week, the pronephros is represented by 7 to 10 solid cell groups in the cervical region.
    These groups form vestigial excretory units, nephrotomes, that regress before more caudal ones are formed.
    By the end of the fourth week, all indications of the pronephric system have disappeared.
  • 8. Relationship of the intermediate mesoderm of the pronephric, mesonephric,
    and metanephric systems.
    In cervical and upper thoracic regions intermediate
    mesoderm is segmented;
    in lower thoracic, lumbar, and sacral regions it forms a solid,
    unsegmented mass of tissue, the nephrogenic cord.
    Note the longitudinal collecting
    duct, formed initially by the pronephros but later by the mesonephros
    Unsegmented mesoderm
    (metanephric system)
  • 9. Excretory
    tubules of the pronephric and mesonephric systems in a 5-week-old embryo.
    Note the longitudinal collecting
    duct, formed initially by the pronephros but later by the mesonephros
    Ureteric bud
  • 10. Mesonephros
    The mesonephros and mesonephric ducts are derived from intermediate mesoderm from upper thoracic to upper lumbar (L3) segments.
    Early in the fourth week, the first excretory tubules of the mesonephros appear.
    They lengthen rapidly, form an S-shaped loop, and acquire a tuft of capillaries that will form a glomerulus at their medial extremity.
    Around the glomerulus the tubules form Bowman’s capsule, and together these structures constitute a renal corpuscle.
    Laterally the tubule enters the longitudinal collecting duct known as the mesonephric or wolffian duct.
  • 11. Transverse section through the urogenital ridge in the lower thoracic region of
    a 5-week embryo showing formation of an excretory tubule of the
    mesonephric system.
    Note the appearance of Bowman’s capsule and the gonadal ridge.
    The mesonephros and gonad are attached to the posterior abdominal wall by a broad urogenital mesentery.
  • 12. Mesonephros
    In the middle of the second month the mesonephros forms a large ovoid organ on each side of the midline.
    Since the developing gonad is on its medial side, the ridge formed by both organs is known as the urogenital ridge.
    The caudal tubules are still differentiating,
    The cranial tubules and glomeruli show degenerative changes, and by the end of the second month the majority have disappeared.
    In the male a few of the caudal tubules and the mesonephric duct persistand participate in formation of the genital system,but they disappear in the female.
  • 13. Relation of the gonad and the mesonephros
    Note the size ofthe mesonephros.
    The mesonephric duct (wolffian duct) runs along the lateral side of the mesonephros
  • 14. MetanephrosThe Definitive Kidney
    The third urinary organ, the metanephros, or permanent kidney, appears in the fifth week.
    Its excretory units develop from metanephric mesoderm in the same manner as in the mesonephric system.
    The development of the duct system differs from that of the other kidney systems.
  • 15. Relation of the hindgut and cloaca at the end of the 5thweek.
    The ureteric bud penetrates the metanephric mesoderm (blastema).
  • 16. 7 weeks
    end of 6th week
    6 weeks
    Newborn
    Note the pyramid form of the collecting tubules entering the minor calyx.
    Development of the
    renal pelvis, calyces, and
    collecting tubules of the metanephros.
  • 17. Collecting System
    Collecting ducts of the permanent kidney develop from the ureteric bud.
    The bud penetrates the metanephric tissue.
    The bud dilates, forming the primitive renal pelvis, and splits into cranial and caudal portions (the future major calyces).
    Each calyx forms two new buds while penetrating the metanephric tissue.
    These buds continue to subdivide until 12 or more generations of tubules have formed.
    Meanwhile, at the periphery more tubules form until the end of the fifth month.
  • 18. Collecting System
    The tubules of the second order enlarge and absorb those of the third and fourth generations, forming the minor calyces of the renal pelvis.
    Collecting tubules of the fifth and successive generations form the renal pyramid.
    The ureteric bud gives rise to the;
    ureter,
    renal pelvis,
    major and minor calyces,
    1 million to 3 million collecting tubules.
  • 19. metanephric excretory unit Development
  • 20. Excretory System
    Each newly formed collecting tubule is covered at its distal end by a metanephric tissue cap.
    Cells of the tissue cap form small vesicles, the renal vesicles,
    Renal vesiclesgive rise to small S-shaped tubules.
    Capillaries grow into the pocket at one end of the S and differentiate into glomeruli.
    These tubules, together with their glomeruli, form nephrons, or excretory units.
    The proximal end of each nephron forms Bowman’s capsule.
    The distal end forms an open connection with one of the collecting tubules, establishing a passageway from Bowman’s capsule to the collecting unit. Continuous lengthening of the excretory tubule results in formation of the proximal convoluted tubule, loop of Henle, and distal convoluted tubule.
  • 21. Excretory System
    The kidney develops from two sources:
    (a) metanephric mesoderm, which provides excretory units.
    (b) the ureteric bud, which gives rise to the collecting system.
    Nephrons are formed until birth, at which time there are approximately 1 million in each kidney.
    Urine production begins early in gestation, soon after differentiation of the glomerular capillaries, which start to form by the10th week.
    At birth the kidneys have a lobulated appearance, but the lobulation disappears during infancy as a result of further growth of the nephrons, although there is no increase in their number
  • 22. Genes involved in differentiation of the kidney
  • 23. Genes involved in differentiation of the kidney(explanation of the figure in the previous slide)
    A. WT1, expressed by the mesenchyme, enables this tissue to respond to induction by the ureteric bud.
    GDNF and HGF interact through their receptors, RET and MET, respectively, to stimulate growth of the bud and maintain the interactions.
    The growth factors FGF2 and BMP7 stimulate proliferation of the mesenchyme and maintain WT1 expression.
    B. PAX2 and WNT4, produced by the ureteric bud, cause the mesenchyme to epithelialize in preparation for excretory tubule differentiation.
    Laminin and type IV collagen form a basement membrane for the epithelial cells.
  • 24. MOLECULAR REGULATION OF KIDNEY DEVELOPMENT
    Differentiation of the kidney involves epithelial mesenchymal interactions.
    Epithelium of the ureteric bud from the mesonephros interacts with mesenchyme of the metanephric blastema.
    The mesenchyme expresses WT1, a transcription factor that
    MAKESthis tissue competent to respond to induction by the ureteric bud,
    REGULATESproduction of glial-derived neurotrophic factor (GDNF) and hepatocyte growth factor (HGF) by the mesenchyme.
    and these proteins stimulate growth of the ureteric buds.
    The tyrosine kinase receptorsRET, for GDNF, and MET, for HGF, are synthesized by the epithelium of the ureteric buds, establishing signaling pathways between the two tissues.
    In turn, the buds induce the mesenchyme via fibroblast growth factor-2 (FGF-2) and bone morphogenetic protein-7 (BMP-7).
  • 25. Both of these growth factors block apoptosis and stimulate proliferation in the metanephric mesenchyme while maintaining production of WT1.
    Conversion of themesenchyme to an epithelium for nephron formation is also mediated by the ureteric buds, in part through modification of the extracellular matrix.
    Thus fibronectin, collagen I, and collagen III are replaced with laminin and type IV collagen, characteristic of an epithelial basal lamina.
    In addition, the cell adhesion molecules syndecan and E-cadherin, which are essential for condensation of the mesenchyme into an epithelium, are synthesized. Regulatory genes for conversion of the mesenchyme into an epithelium appear to involve PAX2 and WNT4.
    MOLECULAR REGULATION OF KIDNEY DEVELOPMENT
  • 26. C L I N I C A L C O R R E L A T E S
    Renal Tumors and Defects
    • Wilms’ tumor =/- (WAGR syndrome is characterized by aniridia, hemihypertrophy, and Wilms’ tumor. Denys-Drashsyndrome consists of renal failure, pseudohermaphrodism, and Wilms’ tumor).
    • 27. Renal dysplasias and agenesis./Potter sequence/ Multicystic dysplastic kidney (Autosomal recessive polycystic kidney disease, autosomal dominant polycystic kidney disease).
    • 28. Duplication of the ureter.
    • 29. one ureter opens into the bladder, and the other is ectopic.
  • partial double ureter
    complete double ureter
    Possible sites of ectopic ureteral openings in the vagina, urethra, and vestibule.
  • 30. POSITION OF THE KIDNEY
    The kidney, initially in the pelvic region,
    later shifts to a more cranial position in the abdomen.
    This ascent of the kidney is caused by diminution of body curvature and by growth of the body in the lumbar and sacral regions.
    In the pelvis the metanephros receives its arterial supply from a pelvic branch of the aorta.
    During its ascent to the abdominal level, it is vascularized by arteries that originate from the aorta at continuously higher levels.
    The lower vessels usuallydegenerate, but some may remain.
  • 31. Ascent of the kidneys
    Gonad descent
  • 32.
  • 33. C L I N I C A L C O R R E L A T E SAbnormal Location of the Kidneys
    During their ascent the kidneys pass through the arterial fork formed by the umbilical arteries, but occasionally one of them fails to do so;
    Pelvic kidney.
    Horseshoe kidney (ascent is prevented by the root of the inferior mesenteric artery).
    Accessory renal arteries (common).
  • 34. FUNCTION OF THE KIDNEY
    The definitive kidney formed from the metanephros becomes functional near the 12th week.
    Urineis passed into the amniotic cavity and mixes with the amniotic fluid.
    The fluid is swallowed by the fetus and recycles through the kidneys.
    During fetal life, the kidneys are not responsible for excretion of waste products,
    The placenta serves this function.
  • 35. BLADDER AND URETHRA 1/2
    During the fourth to seventh weeks of development the cloaca divides into the urogenital sinus anteriorly and the anal canal posteriorly.
    The urorectal septum is a layer of mesoderm between the primitive anal canal and the urogenital sinus.
    The tip of the septum will form the perineal body.
    Three portions of the urogenital sinus can be distinguished:
    The urinary bladder , (the upper and largest part).
    The pelvic part of the urogenital sinus, (narrow canal)
    The phallic part of the urogenital sinus,(flattened from side to side).
  • 36. 8th week
    7thweek
    5th week
    Divisions of the cloaca into the urogenital sinus and anorectal canal. The mesonephric duct is gradually absorbed into the wall of the urogenital sinus, and the ureters enter separately.
  • 37.
    • Initially the bladder is continuous with the allantois,
    but when the lumen of the allantois is obliterated, the urachus, remains and connects the apex of the bladder with the umbilicus.
    In the adult, it is known as the median umbilical ligament.
    • The next part is a narrow canal, the pelvic part of the urogenital sinus,
    • 38. In the male gives rise to the prostatic and membranous parts of the urethra.
    • 39. The last part is the phallic part of the urogenital sinus.
    • 40. It is flattened from side to side, and as the genital tubercle grows, this part of the sinus will be pulled ventrally.
    BLADDER AND URETHRA 2/2
  • 41. During Differentiation of the Cloaca
    The caudal portions of the mesonephric ducts are absorbed into the wall of the urinary bladder.
    The ureters enter the bladder separately.
    As a result of ascent of the kidneys, the orifices of the ureters move farther cranially;
    those of the mesonephric ducts move close together to enter the prostatic urethra and in the male become the ejaculatory ducts.
    The mucosa of the bladder formed by incorporation of the ducts (the trigone of the bladder) is also mesodermal.
    With time the mesodermal lining of the trigone is replaced by endodermal epithelium, so that finally the inside of the bladder is completely lined with endodermal epithelium.
  • 42. Development of the urogenital sinus into the urinary bladder and definitive urogenital sinus.
  • 43. In the male the definitive urogenital sinus develops into the penile urethra.,
    The prostate gland is formed by buds from the urethra
    Seminal vesicles are formed by budding from the ductus deferens.
  • 44. Dorsal views of the bladder showing the relation of the ureters and mesonephric ducts during development
    (C and D)the trigone of the bladder formed by incorporation of the mesonephric ducts.
    (A)Initially the ureters are formed by an outgrowth of the mesonephric duct
    (B–D) with time they assume a separate entrance into the urinary bladder
  • 45. URETHRA
    The epithelium of the urethra in both sexes originates in the endoderm;
    At the end of the third month, epithelium of the prostatic urethra begins to proliferate and forms a number of outgrowths that penetrate the surrounding mesenchyme.
    In the male, these buds form the prostate gland .
    In the female, the cranial part of the urethra gives rise to the urethral and paraurethral glands.
  • 46. Development of the urogenital sinus into the urinary bladder and definitive urogenital sinus.
  • 47. In the male the definitive urogenital sinus develops into the penile urethra.,
    The prostate gland is formed by buds from the urethra
    Seminal vesicles are formed by budding from the ductus deferens.
  • 48. C L I N I C A L C O R R E L A T E SBladder Defects
    Urachal fistula (may cause urine to drain from the umbilicus).
    Urachal cyst(If only a local area of the allantois persists, results in a cystic dilation).
    Urachal sinus(When the lumen in the upper part persists).
    This sinus is usually continuous with the urinary bladder.
  • 49. The sinus may or may not be in open communication with the urinary bladder.
    Urachal fistula
    Urachal cyst
  • 50. Exstrophy of the bladder
    is a ventral body wall defect in which the bladder mucosa is exposed outside.
    This anomaly is rare, occurring in 2/100,000 live births.
    Exstrophy of the Cloaca
    is a more severe ventral body wall defect in which migration of mesoderm to the midline is inhibited and the tail (caudal) fold fails to progress.
    Occurrence is rare (1/30,000),
    defect is associated with early amniotic rupture.
    The defect includes exstrophy of the bladder, spinal defects with or without meningomyelocele, imperforate anus, and usually omphalocele.
  • 51. GENITAL SYSTEM
  • 52. Sex differentiation is a complex process that involves many genes, including some that are autosomal.
    The key to sexual dimorphism is the Y chromosome, which contains the SRY (sex-determining region on Y) gene on its short arm (Yp11).
    The protein product of this gene is a transcription factor initiating a cascade of downstream genes that determine the fate of rudimentary sexual organs.
    The SRY protein is the testis-determining factor; under its influence male development occurs;
    In its absence female development is established.
    GENITAL SYSTEM
  • 53. Influence of primordial germ cells on indifferent gonad
  • 54. GONADS
    The sex of the embryo is determined at the time of fertilization,
    The gonads acquire male or female morphological in the seventh week of development.
    Gonads appear initially as a pair of longitudinal ridges, the genital or gonadal ridges.
    Germ cells appear in the genital ridges in the sixth week of development.
  • 55. Transverse section through the mesonephros and genital ridge
    Relation of the genital ridge and the mesonephros showing location
    of the mesonephric duct
  • 56. A 3-week-old embryo showing the primordial germ cells in the wall of
    the yolk sac close to the attachment of the allantois
  • 57. Migrational path of the primordial
    germ cells along the wall of the hindgut and the dorsal mesentery into the genital ridge
    indifferent gonad
  • 58. Transverse section through the lumbar region of a 6-week embryo showing the indifferent gonad with the primitive sex cords.
    Some of the primordial germ cells are surrounded by cells of the primitive sex cords.
    Shortly before and during arrival of primordial germ cells, the epithelium of the genital ridge proliferates, and epithelial cells penetrate the underlying mesenchyme
    They form the primitive sex cords.
  • 59. TESTIS
    If the embryo is genetically male, the primordial germ cells carry an XY sex chromosome complex.
    The primitive sex cords continue to proliferate and penetrate deep into the medulla to form the testis or medullary cords.
    Toward the hilum of the gland the cords break upinto a network of tiny cell strands that later give rise to tubules of therete testis.
    During further development, a dense layer of fibrous connective tissue, the tunica albuginea, separates the testis cords from the surface epithelium.
  • 60. Transverse section through the testis in the eighth week, showing the tunica albuginea, testis cords, rete testis, and primordial germ cells. The glomerulus and Bowman’s capsule of the mesonephric excretory tubule are degenerating
    Testis and genital duct in the fourth month. The horseshoe-shaped testis cords are continuous with the rete testis cords. Note the ductuli efferentes (excretory mesonephric tubules), which enter the mesonephric duct.
  • 61. In the fourth month, the testis cords become horseshoe shaped, and their extremities are continuous with those of the rete testis.
    Testis cords are now composed of;
    primitive germ cells
    and sustentacular cells of Sertoli derived from the surface epithelium of the gland.
    Interstitial cells of Leydig, derived from the original mesenchyme of the gonadal ridge, lie between the testis cords.
    They begin development shortly after onset of differentiation of these cords.
    By the eighth week of gestation, Leydig cells begin production of testosterone,
    and the testis is able to influence sexual differentiation of the genital ducts and external genitalia.
    TESTIS
  • 62. Testis cords remain solid until puberty, when they acquire a lumen, thus forming theseminiferous tubules.
    Seminiferous tubules are canalized, they join the rete testis tubules,
    Rete testis in turn enter the ductuli efferentes.
    These efferent ductules are the remaining parts of the excretory tubules of the mesonephric system.
    They link the rete testis and the mesonephric or wolffian duct, which becomes the ductus deferens.
    TESTIS
  • 63. Influence of primordial germ cells on indifferent gonad
  • 64. Ovary
    In female embryos with an XX sex chromosome complement and no Y chromosome,
    primitive sex cords dissociate into irregular
    cell clusters.
    The clusters, containing groups of primitive germ cells,
    the clusters Later they disappear
    and replaced by a vascular stroma (forms the ovarian medulla).
    Surface epithelium continues to proliferate.
    In the seventh week, it gives rise to a second generation of cords, cortical cords,
    In the fourth month, these cords split into isolated cell clusters, with each surrounding one or more primitive germ cells.
    Germ cells develop into oogonia,
    the surrounding epithelial cells form follicular cells.
  • 65. Surface
    epithelium
    Degenerating
    mesonephric tubule
    Urogenital
    mesentery
    Degenerating
    medullary
    cords
    Primary
    oocyte
    Cortical
    cords
    Follicular
    cells
    Ductuli efferentes
    Paramesonephric duct
    Mesonephric duct
    Paramesonephric duct
    Surface
    epithelium
    Transverse section of the ovary at the seventh week, showing degeneration
    of the primitive (medullary) sex cords and formation of the cortical cords.
    Mesonephric duct
    Ovary and genital ducts in the fifth month. Note degeneration of the medullary cords.
    The excretory mesonephric tubules (efferent ductules) do not communicate with the rete. The cortical zone of the ovary contains groups of oogonia surrounded by follicular cells.
  • 66. Ovary
    It may thus be stated that the genetic sex of an embryo is determined at the time of fertilization, depending on whether the spermatocyte carries an X or a Y chromosome.
    In embryos with an XX sex chromosome configuration, medullary cords of the gonad regress, and a secondary generation of cortical cords develops.
    In embryos with an XY sex chromosome complex, medullary cords develop into testis cords, and secondary cortical cords fail to develop.
  • 67. Genital ducts in the sixth week in the male (A) and female (B).
    The mesonephric and paramesonephric ducts are present in both.
    Note the excretory tubules of the mesonephros and their relation to the developing gonad in both sexes
  • 68. GENITAL DUCTSIndifferent Stage
    Initially both male and female embryos have two pairs of genital ducts;
    MESONEPHRIC (WOLFFIAN) ducts
    PARAMESONEPHRIC (M¨ ULLERIAN) ducts.
    Cranially the paramesonephric duct opens into the abdominal cavity with a funnel-like structure.
    Caudally the paramesonephric duct first runs lateral to the mesonephric duct, then crosses it ventrally to grow caudomedially.
    In the midline it comes in close contact with the paramesonephric duct from the opposite side. The two ducts are initially separated by a septum but later fuse to form the uterine canal.
    The caudal tip of the combined ducts projects into the posterior wall of the urogenital sinus as (the paramesonephric or m¨ullerian tubercle).
    The mesonephric ducts open into the urogenital sinus on either side of the m¨ullerian tubercle.
  • 69. Abdominal ostium of uterine tube
    Suspensory Ligament of the ovary
    Ligament of the ovary
    fimbriae
    mesovarium
    epoophoron
    paroophoronx
    Corpus uteri
    Cortical cords of the ovary
    Round ligament
    of uterus
    cervix
    mesonephros
    Fornix
    Vagina
    Gartner’s cyst
    Mesonephric duct
    Uterine canal
    Paramesonephric tubercle (m¨ullerian)
    The only parts remaining from the mesonephric system
    are the epoophoron, paroophoron, and Gartner’s cyst
  • 70. Molecular Regulation of Genital Duct Development
    Skip it
  • 71. Influence of the sex glands on further sex differentiation
  • 72. Influence of the sex glands on further sex differentiation
  • 73. Genital Ducts in the Male
    As the mesonephros regresses, a few excretory tubules, the epigenital tubules, establish contact with cords of the rete testis and finally form the efferent ductules of the testis.
    Excretory tubules along the caudal pole of the testis, the paragenital tubules, do not join the cords of the rete testis.
    Their vestiges are collectively known as the paradidymis.
    Except for the most cranial portion, the mesonephric ducts persist and form the main genital ducts.
    the (ductus) epididymis.
    the ductus deferens.
    ejaculatory duct.
    The paramesonephric ducts in the male degenerate except for a small portion at their cranial ends, the appendix testis.
  • 74. the epigenital tubules, establish contact with cords of the rete testis and finally form the efferent ductules of the testis
    Excretory tubules along the caudal pole of the testis, the paragenital tubules, do not join the cords of the rete testis
  • 75. Genital Ducts in the Female
    The paramesonephric ducts develop into the main genital ducts of the female. Initially, three parts can be recognized in each duct:
    Cranial vertical portion that opens into the abdominal cavity,
    Horizontal part that crosses the mesonephric duct,
    Caudal vertical part that fuses with its partner from the opposite side.
    The first two parts develop into the uterine tube
    The caudal parts fuse to form the uterine canal.
    After the ducts fuse in the midline, the broad ligament of the uterus is established,.
    The uterine tube lies in its upper border, and the ovary lies on its posterior surface.
    The uterus and broad ligaments divide the pelvic cavity into the uterorectal pouch uterovesical pouch.
    The fused paramesonephric ducts give rise to the corpus and cervix of the uterus.
    They are surrounded by a layer of mesenchyme that forms the muscular coat of the uterus, the myometrium, and its peritoneal covering, the perimetrium.
  • 76. Urogenital ridge
    Uterorectal pouch
    Mesonephric excretory
    tubule
    ovary
    Mesonephric duct
    Fused paramesonephric ducts
    Broad lig of uterus
    Fused paramesonephric ducts
    paramesonephric duct
    Uterovesical pouch
    C. As a result of fusion, a transverse fold, the broad ligament of the uterus, forms in the pelvis
    . A. and B. The paramesonephric ducts approach each other in the midline and fuse
    Transverse sections through the urogenital ridge at progressively lower levels.
    The gonads come to lie at the posterior aspect of the transverse fold.
  • 77. VAGINA
    The paramesonephric ducts reaches the urogenital sinus , gives rise to the sinovaginal bulbs, which give rise to
    Solid vaginal plate.
    By the fifth month, the vaginal outgrowth is entirely canalized.
    The vaginal fornices, are of paramesonephric origin.
    Thus, the vagina has a dual origin, with the upper portion derived from the uterine canal and the lower portion derived from the urogenital sinus.
    The lumen of the vagina remains separated from that of the urogenital sinus by a thin tissue plate, the hymen.
    The mesonephric duct gives rise to Gartner’s cyst.
    Epoophoron and Paroophoron are remnant of excretory tubule in the mesovarium.
  • 78. 9 weeks. Note the disappearance
    of the uterine septum
    At the end of the third month. Note the tissue of the sinovaginal bulbs
    Newborn
    The fornices and the upper portion of the vagina are formed by vacuolization of the paramesonephric tissue,
    The lower portion of the vagina is formed by vacuolization of the sinovaginal bulbs.
  • 79. Newborn
    Nine weeks
    End of third month
    Sagittal sections showing formation of the uterus and vagina at various
    stages of development.
  • 80. C L I N I C A L C O R R E L A T E SUterine and Vaginal Defects
    Duplications of the uterus
    uterus didelphys
    uterus arcuatus
    uterus bicornis
  • 81.
  • 82. EXTERNAL GENITALIAIndifferent Stage
    In the third week of development, mesenchyme cells originating in the region of the primitive streak migrate around the cloacal membrane to form a pair of slightly elevated cloacal folds.
    The folds unite to form the genital tubercle.
    Caudally the folds are subdivided into urethral folds anteriorly and anal folds posteriorly.
    Another pair of elevations, the genital swellings, becomes visible on each side of the urethral folds. These swellings later form the scrotal swellings in the male and the labia majora in the female.
    At the end of the sixth week, however, it is impossible to distinguish between the two sexes.
  • 83. A and B. Indifferent stages of the external genitalia. A. Approximately
    4 weeks. B. Approximately 6 weeks. C. Scanning electron micrograph of the external
    genitalia of a human embryo at approximately the seventh week. AF, anal fold; arrowhead,
    anal opening; GS, genital swelling; GT, genital tubercle; T, tail; UF, urethral fold.
  • 84. A. Development of external genitalia in the male at 10 weeks. Note the deep urethral groove flanked by the urethral folds. B. Transverse sections through the phallus during formation of the penile urethra. The urogenital groove is bridged by the urethral folds. C. Development of the glandular portion of the penile urethra. D. Newborn.
  • 85. External Genitalia in the Male
    Development of the external genitalia in the male is under the influence of androgens secreted by the fetal testes and is characterized by rapid elongation of the genital tubercle, which is now called the phallus.
    During this elongation, the phallus pulls the urethral folds forward so that they form the lateral walls of the urethral groove.
    This groove extends along the caudal aspect of the elongated phallus but does not reach the most distal part, the glans.
    The epithelial lining of the groove, which originates in the endoderm, forms the urethral plate.
  • 86. At the end of the third month the two urethral folds close over the urethral plate, forming the penile urethra.
    This canal does not extend to the tip of the phallus.
    This most distal portion of the urethra is formed during the fourth month, when ectodermal cells from the tip of the glans penetrate inward and form a short epithelial cord.
    This cord later obtains a lumen, thus forming the external urethral meatus.
    The genital swellings, known in the male as the scrotal swellings, arise in the inguinal region.
    With further development they move caudally, and each swelling then makes up half of the scrotum.
    The two are separated by the scrotal septum.
    External Genitalia in the Male
  • 87. C L I N I C A L C O R R E L A T E SDefects in the Male Genitalia
    Hypospadias
    Epispadias
    Exstrophy of the bladder,
    Micropenis
    Bifid penis or double penis
  • 88. A. Genitalia of a male fetus at 14 weeks, showing fusion of the scrotal
    swellings (S ). Arrow, epithelial tag. B and C. Dorsal and ventral views, respectively, of
    the genitalia of a female fetus at 11 weeks. The genital tubercle at this stage is longer
    than in the male (A), and the genital swellings (GS ) remain unfused.
  • 89. Abnormal
    urethral
    orifices
    Hypospadias showing the various locations of abnormal urethral
    orifices
    Hypospadias
  • 90. Patient with hypospadias. The urethra is open on the ventral surface of
    the penis
  • 91. Mucosa of urinary bladder
    Ureteric opening
    Urethra
    Epispadias combined with exstrophy of the bladder. Bladder mucosa is exposed.
  • 92. External Genitalia in the Female
    Estrogens stimulate development of the external genitalia of the female.
    The genital tubercle elongates only slightly and forms the clitoris.
    urethral folds do not fuse, as in the male, but develop into the labia minora.
    Genital swellings enlarge and form the labia majora.
    The urogenital groove is open and forms the vestibule.
    Although the genital tubercle does not elongate extensively in the female, it is larger than in the male during the early stages of development.
  • 93. Development of the external genitalia in the female at 5 months (A) and in the newborn (B).
  • 94. C L I N I C A L C O R R E L A T E SDefects in Sex Differentiation
    Klinefelter syndrome,
    gonadal dysgenesis/ XY female gonadal dysgenesis (Swyer syndrome)/ Turner syndrome
    Hermaphrodites / pseudohermaphrodites/ Female pseudohermaphroditism is most commonly caused by congenital
    adrenal hyperplasia (adrenogenital syndrome)
    Male pseudohermaphrodites have a 46,XY chromosome complement,
    and their cells are usually chromatin-negative.
    Androgen insensitivity syndrome (formerly testicular feminization)
  • 95. DESCENT OF THE TESTES
    Toward the end of the second month, the urogenital mesentery attaches the
    testis and mesonephros to the posterior abdominal wall (Fig. 14.3A). With degeneration
    of the mesonephros the attachment serves as a mesentery for the gonad . Caudally it becomes ligamentous and is known as the caudal genital ligament . Also extending from the caudal pole of the testis is a mesenchymal condensation rich in extracellular matrices, the gubernaculum. Prior to descent of the testis, this band of mesenchyme terminates in the inguinal region between the differentiating internal and external abdominal oblique muscles. Later, as the testis begins to descend toward the inguinal ring, an extra-abdominal portion of the gubernaculum forms and grows from the inguinal region toward the scrotal swellings. When the testis passes through the inguinal canal, this extra-abdominal portion contacts the scrotal floor (the gubernaculum forms in females also, but in normal cases it remains rudimentary).
    Normally, the testes reach the inguinal
    region by approximately 12weeks gestation, migrate through the inguinal canal
    by 28 weeks, and reach the scrotum by 33 week
  • 96. C L I N I C A L C O R R E L A T E SHernias and Cryptorchism
    The connection between the abdominal cavity and the processus vaginalis in the scrotal sac normally closes in the first year after birth. If remains opened causing a congenital inguinal hernia.
    Sometimes obliteration of this passageway is irregular, leaving small cysts along its course. Later these cysts may secrete fluid, forming a hydrocele of the testis and/or spermatic cord.
    In 97% of male newborns, testes are present in the scrotum before birth.
    In most of the remainder, descent will be completed during the first 3 months postnatally.
    However, in less than 1% of infants, one or both testes fail to descend.
    The condition is called cryptorchidism and may be caused by decreased androgen (testosterone) production. The undescended testes fail to produce mature spermatozoa and the condition is associated with a 3% to 5% incidence of renal anomalies.
  • 97. DESCENT OF THE OVARIES
    Descent of the gonads is considerably less in the female than in the male,
    and the ovaries finally settle just below the rim of the true pelvis. The cranial
    genital ligament forms the suspensory ligament of the ovary, whereas the caudal genital ligament forms the ligament of the ovary proper and the round
    ligament of the uterus (Fig. 14.24). the latter extends into the labia majora.
  • 98.
  • 99. Descent of the testis. A. During the second month. B. In the middle of the third month. Peritoneum lining the coelomic cavity evaginates into the scrotal swelling,
    where it forms the vaginal process (tunica vaginalis).
  • 100. C. In the seventh month.
    D. Shortly after birth
  • 101.
  • 102. A. Testis, epididymis, ductus deferens, and various layers of the abdominal wall that surround the testis in the scrotum. B. Vaginal process in open communication with the peritoneal cavity. In such a case, portions of the intestinal loops often descend toward and occasionally into the scrotum, causing an inguinal hernia. C. Hydrocele.
  • 103. Kidney develop
    Ureter develop
    Failure of the allantois to obliterate will lead to urachal fistula/ cyst/ sinus
    Horseshoe kidney lies in cavity