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PEDIATRICS: EXTERNAL GENITAL ANOMALIES IN BOYS

Normal Male External Genitalia

Embryology

At 9-13 weeks of gestation, dihydrotestosterone (DHT) simulates androgen receptors the
1. Genital tubercle to differentiate into penis
2. Urethral folds to differentiate into the corpus spongiosum/penile shaft
3. Labioscrotal swellings to differentiate into scrotum

Also known as genital swellings or labioscrotal folds§

The male develops in a proximal-to-distal manner
As the penis forms from the elongation and enlargement of the phallus, the lateral walls of the urethral groove form from the ventrally located urethral folds, which then fuse in the midline.
The scrotum forms from midline fusion of the labioscrotal swellings as delineated by the scrotal raphe.

By the end of the first trimester (12 weeks), the external genitalia are completely masculinized
- US sex determination after 13 weeks is accurate in 99-100% of cases of gestation without malformed external genitalia
In females and males with abnormalities in testosterone and/or DHT production, 5α-reductase deficiency, or androgen-receptor insufficiency, the
1. Genital tubercle passively become the clitoris
2. Urethral folds passively become the labia minora
3. Labioscrotal swellings passively become the labia majora

See Table 146-3: Tanner Classification of Sexual Maturity Stages in Boys

Penile Anomalies

Prepuce (Foreskin)

Phimosis

See CUA Circumcision Guidelines

Paraphimosis

In most cases, manual compression of the glans with placement of distal traction on the edematous foreskin allows reduction of the paraphimotic ring

Source: Bangs, Lemuel Bolton. An American text-book of genito-urinary diseases, syphilis and diseases of the skin. WB Saunders, 1898.

Other options include:
1. Application of an iced glove for 5 minutes
2. Application of granulated sugar for 1-2 hours
3. Placement of multiple punctures in the edematous skin

Circumcision

See CUA Circumcision Guidelines
Potential benefits:
1. Reduced risk of Penile cancer
2. Reduced risk of UTIs
3. Reduced risk of Sexually transmitted diseases including HIV
4. Reduced risk of Phimosis
5. Reduced risk of Balanitis
Contraindications (2):

Neonates with other penile conditions (hypospadias, penile curvature, dorsal hood deformity, buried penis, and webbed penis) that require surgical correction

Other conditions commonly seen in neonates that should be taken into consideration are a large hydrocele or inguinal hernias, which are more likely to develop secondary phimosis, buried penis, and trapped penis.
There should be complete separation of the prepuce from the glans and complete inspection of the meatus and the corona to confirm the absence of anomalies, including hypospadias.

Coagulopathy

Techniques and devices for neonatal circumcision:
1. Gomco clamp
2. Mogen clamp
3. Plastibell device
Complications (6):

Risk of complications after circumcision: 0.2-5%

Bleeding

Most common complication, occurs in 0.1% and is more common in older children
Usually localized from the frenulum

Wound infection

Rare complication
Antibiotic ointment (e.g., bacitracin) after circumcision usually prevents its development

Penile skin complications

Insufficient or asymmetrical excision can result in a cosmetic and social dilemma for the parents and child
Excessive skin excision can result in:
1. Penile chordee, torsion, and lateral deviation
2. Trapped penis from a cicatricial scar

Glanular adhesions and skin bridges

Glanular adhesions and skin bridges, attachments of the glans and penile shaft, respectively, are common complications
Both can occur in the well-circumcised penis and are usually the result of the physiologic retraction of the penis caused by a suprapubic fat pad and diaper irritation of the penis
Management
- Persistent adhesions can be lysed in the office with the application of a topical analgesic such as EMLA cream
- Low-dose corticosteroids have been relatively unsuccessful in lysing adhesions

Meatal Stenosis

The normal urethral meatus is:

Age<4: 10 Fr
Age 4-10: 12 Fr
Age>10: 14 Fr

Symptoms include:
1. Narrow, high-velocity stream
2. Urinary stream deviation, typically in an upward direction resulting from a meatal baffle or ventral web located at the inferior aspect of the meatus
3. Penile pain at the initiation of micturition

Penile Trauma

Most serious complication
Includes urethral injury, excision of the glans and/or penile shaft, and penile necrosis

Urethral injury requires urethroplasty
Excision of the glans can be repaired by suturing the excised tissue back to the penis, often without the need for microscopic repair
- Good results if performed within 8 hours

Lichen sclerosis (Balanitis Xerotica Obliterans)

See Penis and Urethra Surgery Chapter Notes
Rare in children age <5 years
At puberty, inability to retract the prepuce is the most common presentation
Other presenting symptoms include:
- Local infection
- Irritation
- Discomfort after micturition
- Bleeding
- Occasionally acute urinary retention or urinary incontinence
Circumcision is the preferred treatment along with meatotomy or meatoplasty if there is meatal involvement

Children with meatal involvement should be observed post-operatively because of the risk of recurrent meatal stenosis
The use of topical corticosteroids has had limited benefit to treat mild BXO of the prepuce with minimal scar formation

Abnormal Penile Number

Aphallia

Penile agenesis results from failure of development of the genital tubercle
The karyotype almost always is 46,XY, and the usual appearance is that of a well-developed scrotum with descended testes and an absent penile shaft.
Associated malformations are common and include cryptorchidism, vesicoureteral reflux, horseshoe kidney, renal agenesis, imperforate anus, and musculoskeletal and cardiopulmonary abnormalities
Testing should include a karyotype and other appropriate studies to detect associated malformations of the urinary tract or other organ systems.
- MRI may be beneficial in determining the severity of the defect

Diphallia

Duplication of the penis is a rare anomaly; incidence of 1 in 5 million live births

Abnormal penile size

Normal penile size in a full-term male neonate
- Stretched length: 3.5cm (13.3cm in adults)
- Diameter: 1.1cm
Inconspicuous Penis

Definition of inconspicuous penis: penis that appears to be small but with normal stretched penile length measured from the pubic symphysis to the tip of the glans and normal diameter of the penile shaft

Differentiated from micropenis, in which the penis is abnormally small

Subtypes (3): buried penis, webbed penis, and trapped penis
- Buried Penis
  - Definition of a buried penis: a normally developed penis that is hidden away by a suprapubic fat pad
  - Classified into 3 categories based on cause of the concealment:
    1. Poor penopubic fixation of the skin at the base of the penis
    2. Obesity
    3. A trapped penis from cicatricial scarring after penile surgery, typically a circumcision
      - May occur after neonatal circumcision in an infant with significant scrotal swelling as a result of a hernia or hydrocele or after routine circumcision in an infant with a webbed penis

Buried penis due to obesity

Source: Wikipedia

Management
- Based on the cause
- The trapped penis can be managed with betamethasone, vertical relaxation incision, and formal repair

Webbed Penis
- Definition of a webbed penis: a congenital or acquired condition resulting from the scrotal skin extending onto the ventrum of the penis
- Also known as penoscrotal fusion

Webbed penis

Source: Wikipedia

Micropenis
- Definition of micropenis: a normally formed penis that is at least 2.5 standard deviations (SD) below the mean size in stretched length for age
  - Stretched penile length correlates more closely with erectile length than does the relaxed penile length and should be compared with standards for penile length
  - Micropenis in the full-term neonate is stretched penile length <1.9 cm long
- Causes
  - See CW11 Box 146-1: Etiology of Micropenis
  - Results from a hormonal abnormality that occurs after 14 weeks of gestation
  - Hypogonadotropic hypogonadism (most common cause)
    - Failure of the hypothalamus to produce adequate quantities of gonadotropin-releasing hormone (GnRH) can occur in Prader-Willi syndrome, Kallmann syndrome (genital-olfactory dysplasia), Laurence-Moon-Biedl syndrome, and the CHARGE association
  - Hypergonadotropic hypogonadism (primary testicular failure)
  - Idiopathic
  - Often associated with major chromosomal defects, including: Klinefelter syndrome (47,XXY) and other X polysomy syndromes, deletions, translocations, and trisomy involving chromosomes 8, 13, and 18
- Initial evaluation of a child with micropenis includes a history, physical examination, and a karyotype at birth.
- The ratio of the length of the penile shaft to its circumference is usually normal, but occasionally the corpora cavernosa are severely hypoplastic. The testes are usually small and frequently cryptorchid, whereas the scrotum is usually fused and often diminutive
- Although ultimate penile size may be below the normal range, men born with micropenis have male gender identity and most have satisfactory sexual function

Adult male with micropenis (flaccid left, erect right)

Source: Wikipedia

Abnormal Penile Orientation
- Congenital penile curvature
  - Referred to as chordee
  - Results from disproportionate development of the tunica albuginea of the corporal bodies
    - Not associated with urethral malformation§
  - Most commonly in the ventral direction (as opposed to Peyronie’s which is dorsal curvature), with preserved penile length and typically normal erectile function and rigidity§
  - Commonly associated with hypospadias
    - Isolated chordee may occur with or without a dorsal hood of prepuce and is commonly associated with a deficiency of the ventral skin
  - Congenital dorsal penile curvature may be an isolated condition with or without asymmetrical penile skin or associated with epispadias and a ventral hood of prepuce.
  - Healthy young men usually present between age 18-30 when the abnormal curvature is brought to their attention from their sexual partner
  - Treatment is surgical and is offered to patients whose congenital penile curvatures significantly interferes with satisfactory sexual relations of the patient or partner.
    - Plication is used almost exclusively§
- Penile Torsion
  - Definition of penile torsion: a rotational deformity of the penile shaft, usually in the counterclockwise direction
  - The cause has not been clearly delineated but may be the result of an anomalous arrangement of penile shaft skin.
Penile Masses (5):
1. Penile cysts
  - Most common penile mass in children
  - Can be congenital or acquired
2. Parameatal Urethral Cyst
  - A rare anomaly and appears as a small blister in proximity to the urethral meatus
3. Inclusion Cysts
  - Smegma pearl
    - Smegma, produced under the foreskin, is made of 27% fat and 13% protein§
    - A smegma pearl is a type of inclusion cyst where smegma becomes entrapped under the unretractable foreskin
      - See Figure
    - Most common acquired cystic lesion of the penis
  - May form after penile surgery, including circumcision and hypospadias repair, owing to islands of epithelium within the subcutaneous tissue. Excision of the epidermal inclusion is recommended.
4. Congenital Penile Nevi
  - Pigmented lesions that can form on the glans and penile shaft tend to be superficial and benign and should be excised
5. Juvenile Xanthogranuloma
  - Uncommon benign lesion of the penis
  - Lesions appear as solitary or multiple pigmented (yellow, orange, gold, brown, or red) nodules of rapid onset. They measure 2-20 mm in diameter and are well demarcated, firm, and rubbery.
  - Predominantly seen in infancy or early childhood.
  - The lesion is often self-limited, and a period of 1 year of expectant monitoring is advised to avoid potentially unnecessary ablative genital surgery
Accessory Urethral Openings
- Congenital Urethral Fistula
- Urethral Duplication
  - Duplication most commonly occurs in the sagittal plane with one urethra located ventrally and the other dorsally
    - Usually the dorsal urethra is considered the accessory urethra with or without a urinary stream, whereas the ventral urethra carries the urine stream and the anatomic landmarks such as the external sphincter and verumontanum.
  - Associated genitourinary, gastrointestinal, and musculoskeletal anomalies may be present
    - Vesicoureteral reflux is the most common associated anomaly
    - Other anomalies include renal agenesis, bilateral cryptorchidism, sacral agenesis, imperforate anus, radial hypoplasia, tracheoesophageal fistula, and other midline defects such as duplicated bladder, duplicated colon, imperforate anus and anorectal agenesis, bifid glans, thoracic hemivertebrae, and partial sacral agenesis
  - The most common presentation of urethral duplication is a double meatus and double urinary stream
  - Evaluation should include a voiding cystourethrogram, retrograde urethrogram, and direct visualization of the anatomy during cystourethroscopy
Genital Lymphedema

A disfiguring disorder characterized by impaired lymphatic drainage that causes progressive penile or scrotal swelling

Can be congenital or acquired

Priapism

Stuttering, low-flow, high-flow priapism

See Priapism Chapter Notes

Spontaneously resolving priapism

Form observed in neonates

Causes may include idiopathic factors, birth trauma, and polycythemia

No intervention is necessary because the priapism usually resolves in 2-6 days without adverse results

Penoscrotal Transposition (Scrotal Engulfment)

Frequently occurs in conjunction with perineal, scrotal, or penoscrotal hypospadias with chordee

Also associated with caudal regression, sex chromosome abnormalities, and Aarskog syndrome.

As many as 75% of patients with complete penoscrotal transposition and a normal scrotum have a significant urinary tract abnormality, including renal agenesis and dysplasia, and other nongenitourinary anomalies

Scrotal Anomalies

Bifid Scrotum

Deformity in which the labioscrotal folds are completely separated and without a median raphe
Most often associated with proximal hypospadias

Ectopic Scrotum

The anomalous position of one hemiscrotum along the inguinal canal
- Possible locations: suprainguinal (most common), infrainguinal, or perineal
Rare condition
Associated with cryptorchidism, inguinal hernia, bladder exstrophy, popliteal pterygium syndrome
Patients should undergo upper urinary tract imaging with US

Scrotal Hypoplasia

Underdevelopment of one or both sides of the scrotum
Occurs most commonly in boys with an undescended testis

Scrotal Agenesis
Scrotoschisis

See Figure
When scrotoschisis is detected the clinician should suspect meconium peritonitis
Treatment involves scrotal exploration with orchiopexy and primary closure of the scrotal wall defect

Vascular Lesions of the Genitalia

Congenital Cutaneous Hemangiomas

Although the lesions may undergo a period of rapid growth lasting 3 to 6 months, gradual involution is common, and most lesions require no treatment

Subcutaneous/Cavernous Hemangiomas

In contrast to cutaneous hemangiomas, which tend to involute, cavernous hemangiomas tend to enlarge gradually and should be treated with care.
Definitive treatment by en bloc resection is advised

Hernia and Hydroceles

Embryology

The processus vaginalis forms during the 3rd month of gestation as the peritoneum bulges into the inguinal canal just before the onset of testicular descent.

On completion of testicular descent, the processus vaginalis obliterates and the portion adjacent to the testes becomes the tunica vaginalis
Obliteration of the processus vaginalis continues post-natally, and its failure to obliterate accounts for nearly all inguinoscrotal abnormalities seen in infancy and childhood

Patent process vaginalis is associated with (4):
1. Transverse testicular ectopia
2. Epididymal anomalies
3. Cryptorchidism
4. Polyorchidism
- Risk of spermatic cord torsion is associated with abnormal development of the tunica vaginalis but not patency of the processus vaginalis
Incidence of incidental patency observed in older children and adults at autopsy or laparoscopy is ≈20%

Definitions

Indirect inguinal hernia: a widely patent processus vaginalis extending beyond the internal inguinal ring containing abdominal contents (bowel, omentum, gonads) which may pass into the inguinal canal, labia, or scrotum
Communicating hydrocele: a patent processus vaginalis extending beyond the internal inguinal ring containing peritoneal fluid alone, which extends to the testis, with fluid within the tunica vaginalis
Hydrocele of the spermatic cord: fluid contained within a segment of patent processus vaginalis with obliterated processus distally and proximally
Scrotal hydrocele: fluid contained within the tunica vaginalis surrounding the testis without communication proximally
- May be seen as a chronic or acute scrotal swelling after an inflammatory, infectious, or traumatic event. The hydrocele size is typically stable but may decrease over time.
Abdominoscrotal hydrocele: a large scrotal hydrocele that extends proximally across the internal inguinal ring into the abdomen without communication with the peritoneum
- Associated with (4):
  1. A closed processus vaginalis.
  2. Testicular dysmorphism.
  3. Hydronephrosis.
  4. Increased pressure within the tunica vaginalis.

Epidemiology and Pathogenesis

Inguinal Hernia and Communicating Hydrocele

Inguinal hernias develop in 1-5% of children, 5-10x more common in boys and significantly more common among premature infants
More common (3:1) on the right side
- Attributed to the later descent of the right testicle
Risk factors for bilateral involvement (4):
1. Female gender
2. Prematurity
3. Age < 1
4. History of cryptorchidism
Average age at presentation is 3-4 years
The majority of new hydroceles occurring after birth and before puberty are associated with a patent processus vaginalis (clinically communicating, clear history of fluctuation)

Noncommunicating Hydroceles

Hydroceles that spontaneously resolve during infancy or appear during or after puberty are more commonly non-communicating
These form from delayed fluid absorption or abnormal fluid dynamics within the tunica vaginalis

Diagnosis and Evaluation

History and Physical Exam

History
- Typically manifests as a painless bulge found in the groin or extending along the cord to the scrotum.
  - The bulge may be present only during periods of increased intra-abdominal pressure (crying or bowel movements
    - The presence of an intermittent bulge helps to distinguish a reducible inguinal hernia and communicating hydrocele from a scrotal hydrocele or hydrocele of the spermatic cord.
    - The child with an incarcerated inguinal hernia will be irritable or inconsolable and have a persistent or larger bulge without spontaneous reduction and may have decreased appetite and signs of bowel obstruction (abdominal distention, vomiting, and lack of flatus or stool)
Physical Exam
- The supine position facilitates reduction of peritoneal fluid and intra-abdominal contents
- The hydrocele fluid surrounding the testicle should transilluminate; however, neonatal bowel may also transilluminate.
- The hydrocele of the spermatic cord is usually painless and variable in size. It may be confused for the testis because of its round-oval shape

Imaging

Often of limited use

Management

Hydroceles

Both communicating and non-communicating hydroceles may resolve spontaneously in infants (CW12 p392 and CW11)

No indication for surgery within the first 24 months of age
- Indications for intervention:
  - Hydrocele associated with inguinal hernia
  - Hydrocele develops when child is several years old
  - Hydrocele enlarges during the period of observation

Inguinal Hernia

Require surgical repair shortly after diagnosis, given the significant risk of associated complications
Standard Inguinal Hernia Repair
- The traditional surgical approach to repairing an indirect inguinal hernia or communicating hydrocele is high ligation of the hernia sac at the level of the internal inguinal ring. This carries a high success rate
- In peripubertal boys with hydrocele, determine if hydrocele is communicating or scrotal.
  - If communicating, inguinal approach is preferred
  - If scrotal, trans-scrotal hydrocele approach is performed as in adults and an inguinal incision made only if a proximal communication is identified.
- Complications
  - Early postoperative complications, including bleeding and infection, are rare after standard hernia repair
  - Recurrent inguinal hernia
    - Rate after uncomplicated open repair: 0.5-1%
    - Causes include failure to properly identify or ligate the sac during the original procedure; a tear in the sac, leaving a strip of peritoneum along the cord; damage to the floor; or a missed direct hernia at the original exploration.
    - Laparoscopic inguinal hernia repair associated with higher risk of recurrence (up to 4%) than with open repair
  - Secondary cryptorchidism, testicular atrophy, and vasal injury is not well defined.
    - If a testis is incompletely descended or retractile, orchidopexy should be performed at the time of herniorrhaphy
Assessment of the contralateral internal ring
- The need to assess the patency of the contralateral processus vaginalis or of the internal inguinal ring in children with a unilateral hernia remains controversial

Acute Scrotum

Refers to the constellation of new onset of pain, swelling, and/or tenderness of intrascrotal contents.
Differential diagnosis (see CW11 box 146-2)

Torsion of the appendix testis is the most common diagnosis followed by spermatic cord torsion, epididymitis

Although all of these diseases can occur at any time during childhood,
- Torsion of the appendix testis is typically most common after infancy and before puberty
- Epididymitis and spermatic cord torsion are most common in the perinatal and pubertal periods
Torsion of an appendage and epididymitis are managed conservatively with limited consequence
Prompt surgical exploration for spermatic cord torsion is imperative because the gonad is at considerable risk of ischemic damage or loss

Spermatic Cord Torsion

Acute Intravaginal Spermatic Cord Torsion

Left-sided predominance
Epidemiology
- May occur at any age, but the vast majority of cases occur after age 10 years with a peak at age 12-16 years
Predisposing Factors

Commonly attributed to excess mobility of the testis within a “bell-clapper deformity”, wherein the tunica vaginalis abnormally fixes proximally on the cord
Familial predisposition
Cryptorchid testes

Diagnosis and Evaluation

History and Physical Exam
- History
  - The inciting event for torsion is unknown
  - History of prior episodes may be elicited
  - Nausea/vomiting occurs in 10-60% of boys
  - Dysuria and fever are uncommon
- Physical exam
  - The most common physical findings are:
    - Generalized testicular tenderness
    - Abnormal (horizontal) orientation of the testis
    - High-riding testis from a foreshortened cord
    - Absent cremasteric/genitofemoral reflex
      - Elicited by scratching the inner thigh with resultant testis elevation
      - Normally present age >2 years
      - Some studies report reduced or absent reflex in all cases of testicular torsion, but intact in up to 10% of proven cases of torsion in other series
  - Scrotal edema and erythema may be present, depending on the duration or degree of torsion.
Imaging
- Before the advent of reliable and rapid scrotal imaging, immediate scrotal exploration was routine
- CDUS findings consistent with testicular torsion include:
  1. Reduced or absent Doppler color or waveforms
  2. Parenchymal heterogeneity compared with the contralateral testis

Management

Surgical emergency
Risk of orchiectomy based on onset of pain

0-6 hours: 5%
7-12 hours: 20%
13-18 hours: 40%
19-24 hours: 60%
24-48 hours: 80%
>48 hours: 90%

Irreversible ischemic injury to the testicular parenchyma may begin as soon as 4 hours after occlusion of the cord.
Manual detorsion can be attempted. However, manual detorsion may not totally correct the rotation that has occurred and that prompt exploration is still indicated
The testis is untwisted, wrapped in warm soaked gauze, and observed for improvement in color while the contralateral testis is fixed with nonabsorbable suture to reduce the risk of metachronous torsion.
- Median degree of rotation was 540° in orchiectomy testes and 360° when the testis was salvaged
- If the testis is to be retained, it is fixed either via dartos pouch or directly to the dartos with nonabsorbable suture.
- In cases of orchiectomy, prosthesis placement is usually offered after complete healing or later in puberty

Prognosis

Subtle abnormalities of semen quality are common

Semen density is often within the normal range

Global testicular dysfunction may exist after torsion

May be due to ischemia-reperfusion injury after release of testicular torsion

Hypothesis of an autoimmune phenomenon has been dispelled

Serum FSH, LH, and testosterone were within the reference range.

Intermittent Intravaginal Spermatic Cord Torsion

Scrotal swelling or nausea and/or vomiting may or may not be present
A normal vertical testicular orientation is most common
Whirlpool sign or an abnormal boggy cord and pseudomass formation below the twisted spermatic cord may also signify intermittent torsion
Diagnosis requires a high index of suspicion unless the testis is noted to untwist
Once the condition is confirmed or highly suspected, elective bilateral orchidopexy is indicated to avert torsion and possible organ loss.
Patients and parents should know that absolute confirmation of the diagnosis may not be possible and that symptoms may persist postoperatively.

Extravaginal Spermatic Cord Torsion (Perinatal Testicular Torsion)

Perinatal spermatic cord torsion is a term applied to infants regardless of whether the event occurred prenatally (hours, days, weeks, months), during delivery, or postpartum.
Torsion of the entire cord occurs before fixation of the tunica vaginalis and dartos within the scrotum (extravaginal).
Most commonly occurs well before delivery, yielding a “vanishing” testis or a hemosiderin-containing nubbin in the scrotum or less commonly in the inguinal canal.
The testis that sustains loss of blood supply close to delivery is a hard, painless testis fixed to the overlying erythematous or dark scrotal skin with or without edema
[Urgent exploration is not needed.] However, if torsion is suspected after a normal postnatal scrotal examination, then prompt exploration should be performed as for intravaginal torsion. If torsion is confirmed, contralateral scrotal exploration with testicular fixation should be performed.

Torsion of the Appendix Testis and Epididymis

Appendix testis

From the müllerian duct
Present in 76-83% of testes

Appendix epididymis

From the wolffian duct
Present in 22-28% of testes

The peak age at occurrence is 7 to 12 years
Diagnosis and Evaluation
- History and Physical Exam
  - Physical Exam
    - A “blue dot sign”, a discoloration at the upper pole of the testis representing the ischemic appendage, may be seen through stretched scrotal skin
- Imaging
  - US
    - The normal appendix testis contains no internal blood flow, whereas the twisted appendage may appear as an ovoid hyperechoic, hypoechoic, or heterogeneous nodule without blood flow
    - CDUS rarely demonstrates an abnormal appendage but commonly shows hyperperfusion of the epididymis.
Managment
- Torsion of an appendage is a self-limited process; surgery is rarely indicated

Epididymitis

Symptoms have a more insidious onset than torsion of the cord or an appendage but may be present rapidly
The cremasteric reflex should be intact
The majority of infants with epididymitis have sterile urine and apparently radiographically normal urinary tracts.
The management goal is to relieve inflammation and any associated infection
In a prepubertal child with a positive urine culture, renal US and VCUG are indicated (different than elsewhere that only describe a renal US for child with first UTI)

Varicocele

See Varicocele Chapter Notes

Epididymal cysts

Simple cystic structures that may be palpable by the patient or examining physician or found incidentally by US
Pathophysiology is unknown but may be related to an altered hormonal environment because they are linked to diethylstilbestrol (DES) exposure
Management
- Many resolve spontaneously; surgical intervention is rarely needed

Vasal Anomalies

Congenital absence of the vas deferens (CAVD) is in most cases associated with specific mutations of the cystic fibrosis gene CFTR (cystic fibrosis transmembrane regulator) that are less severe than those encountered in patients with cystic fibrosis.

Disease can be bilateral (CBAVD) or unilateral (CUAVD) with a normal or obstructed contralateral vas
May be associated with renal agenesis or ectopia and/or partial or complete agenesis of the epididymis and seminal vesicles

Questions

List contraindications to circumcision
What is the differential diagnosis of a penile mass in a child?

Answers

List contraindications to circumcision
What is the differential diagnosis of a penile mass in a child?

References

Wein AJ, Kavoussi LR, Partin AW, Peters CA (eds): CAMPBELL-WALSH UROLOGY, ed 11. Philadelphia, Elsevier, 2015, vol 4, chap 146