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Prostate
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Inflammatory
- Acute bacterial prostatitis
- Chronic bacterial prostatitis
- Chronic abacterial prostatitis/prostatodynia - CHRONIC PELVIC PAIN SYNDROME
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Tumors
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Nodular hyperplasia/Benign prostatic hyperplasia
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General
- Very common (20% 40's - 70% of 60's)
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Pathology
- Nodular hyperplasia, stroma&glands
- double layer of epithelium preserved
- Transition zone (Normally 5% of prosttatic volume , in BPH up to 95%)
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Carcinoma
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General
- Very common, age (20%-50's, 70%-70's)
- Latent vs clinically significant
- Problem of overtreatment
- LATENT: low grade, low volume, low PSA
- DRE/PSA
- Utility & Limitations
- reference values
- the total PSA range of 4.0 to 10.0 ng/mL has been described as a diagnostic "gray zone,"
- false+ & false- results
- PSA derivatives & kinetics
- not specific for disease progression
- free: total PSA (F/T ratio)
- density
- velocity - the rate of change in PSA level
- doubling time
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Pathology
- Adenocarcinoma
- small infiltrating glands, architectural distortion
- single layer of cells
- large nuclei with prominent nucleoli
- AdenoCa, LOW MAG
- AdenoCa, High MAG
- Gleason grading
(a method to grade differentiation
of prostate carcinoma)
- Architectural patterns
- 3 - donuts
- 4 - pretzels
- 5 - solid sheets or single cells
- GLEASON SCORE
- sum of the two most prevelent patterns
- Peripheral zone (70% OF GLAND VOLUME, 80% OF CANCERS)
- Precursors: HGPIN, Adenosis (AAH)
- stong association but the risk of progression unknown
- Spread
- Role of pathologists
- Biopsy, core bx
- diagnosis
- GS prognostic grouping
- I - 3+3
- II - 3+4
- III - 4+3
- IV - 4+4
- V - 4+5, 5+4; 5+5
- GS and tumor volume
- Key factors in management of patients
- together with age, PSA level, clinical stage
- Transurethral resection of prostate (TURP)
- exclusion of neo
- Radical prostatectomy
- Pathological Stage (pTNM)
- Gleason score
- Margin status
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Anatomy & histology
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Zonal anatomy
- Zonal anatomy
- Histology
- Histology
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Testis & paratesticular tissues
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Congenital anomalies
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Testicular dysgenesis
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abnormal embryonic development of gonads (hypoplastic or incompletely developed + hypogonadism)
- result in DISORDERS OF SEX DEVELOPMENT
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Cryptorchidism
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component of Testicular Dysgenesis Syndrome
- TDS spectrum
- ENDOCRINE DISRUPTORS
- Xenoestrogens: , PCB, Bisphenol A, Phtalates
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NON-PALPABLE ABSENT TESTICLE/TESTES IN THE SCROTUM
(EMPTY SCROTUM)
- un-/maldescended, ectopic, regressed or missing (anorchia)
- atrophy or fibrous streak or complete lack of testicular structures
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Vanishing testes syndrome/testicular regression syndrome
- At least 5% of cryptorchid testes
- "vascular accident"(va) during emryo or fetal development leading to disapperance of initially normal testicle
- phenotype depends on the time of the va - variants from unilateral anorchia through ambiguous gentilia to female internal& external phenotype
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ORCHIOPEXY to prevent complications
- infertility (<2yo)
- germ cell tumors (<5yo)
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Inflammatory
- Infectious (Non-specific Gram- bacilli and pyogenic cocci, viruses or STD)
Non-infectious (vasculitis, trauma, idiopathic)
- Epididymo-orchitis
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Epididymitis
- Tuberculosis
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Orchitis
- viral: mumps
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Vascular
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Torsion
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anomalous testicular suspension defect
- torsion
- incompletely descended testis is more prone to torsion during the fetal period
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Tumors
- GERM CELL NEOPLASIA IN SITU (GCNIS)
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Neoplasms
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Germ cell tumors (GCTs) >95%
- General
- Most common cancer in young males
- Aggresive but curable
- AGE DIFFERENCES
- Biomarkers: AFP, bHCG, LDH
- Pathology
- Pure (40%)
- Seminoma (>90% of pure, 35-40% of all)
- seminoma
- Non-seminomatous
- Embryonal carcinoma
- EC
- Yolk sac tumor
- YST
- Choriocarcinoma
- CCH
- Teratoma
- Dermoid cyst
- Mixed most common (60%)
- Precursor: IGCN
- Spermatocytic seminoma/SPERMATOCYTIC TUMOR
- distinct entity, different molecular pathway, elderly
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Sex cord stromal tumors <5%
- Leydig cell tumor (most common SCST)
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Secondary
- Lymphoma (most common testIcular neo in >60 yo)
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Celes and cysts
of spermatic cord & adnexa
- HYDROCELE
- SPERMATOCELE
- VARICOCELE
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Differential diagnosis
- Epidymoorchitis
- Inguinal hernia
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HYPOGONADISM
(gonadal failure)
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PRIMARY (hypergonadotropic)
- genetic syndromes
- maldescended testes
- vanishing testes syndrome
- external insults (eg inflammation, ischaemia)
- autoimmune
- Sertoli cell only syndrome
- SECONDARY (hypogonadotropic)
- presentation depends on the age of development
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Anatomy & histology
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testis
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seminiferous ducts
- seminiferous ducts
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Penis & Urethra
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Structural/Congenital Abnormalities
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Abnormal urethral groove/canal
- Hypospadias
- Epispadias
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Phimosis
- Paraphimosis
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Inflammatory
- Infectious (Non-specific or STD)
Non-infectious (Lichen sclerosus et atrophicus/BXO)
- Balanoposthitis (glans&prepuce)
- Urethritis
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Neoplasms
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Benign
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Condyloma acuminatum/anogenital wart
- wart
- wart
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Preinvasive/precursor lesions -PENILE INTRAEPITHELIAL NEOPLASIA (PeIN)
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Clinical presentations (variable)
- HPV-related (oncogenic, high-risk types)
- Bowenoid papulosis - transitional state between a genital wart and Bowen disease,
pigmented papules on the shaft, spontaneous regression, younger (30's-40's)
- Bowen's disease - scaly hyperkeratotic plaque, usually on shaft of penis
- Erytroplasia of Queyrat - erythematous plaque on the glans and prepuce
- HPV-unrelated
- Phimosis with leukoplakia - whitish patch or plaque on the glans or prepuce
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Pathology (common)
- 1.TRANSEPIDERMAL CYTOLOGICAL ATYPIA, 2.ABNORMAL PROLIFERATION, 3.ABNORMAL MATURATION
- PeIN, histopatho
- HPV-related (particularly (HPV-16 and 18), looks like HGPIN in cervix
- not related to HPV
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Malignancy
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Squamous cell carcinoma
- 0,5% of male cancers, >50yo
- 70% HPV-unrelated, 30% HPV-related
- Verrucous carcinoma
- special subtype with good prognosis
- Clinical&HP
- Other possible skin tumors: melanoma, Paget's disease, basal cell carcinoma