Medicine /USMLE - Reproduction Part 2

USMLE - Reproduction Part 2

Medicine100 CardsCreated 4 days ago

**Cleft Lip** is a congenital anomaly resulting from the **failure of fusion between the maxillary and medial nasal processes** during embryonic development. This defect affects the formation of the **primary palate**, leading to a gap or split in the upper lip, which may be unilateral or bilateral.

Ketoconazole

Kind of drug

MoA

Uses

Toxicity

Antiandrogen
Inhibits steroid synthesis (--/ 17,20 desmolase)
Treats PCOS to prevent hirsutism
Tox: gynecomastia and amenorrhea

Tap or swipe ↕ to flip
Swipe ←→Navigate
SSpeak
FFocus
1/100

Key Terms

Term
Definition

Ketoconazole

Kind of drug

MoA

Uses

Toxicity

Antiandrogen
Inhibits steroid synthesis (--/ 17,20 desmolase)
Treats PCOS to prevent hirsutism
Tox: gynecomastia and amenorrhea

Spironolactone

Kind of drug

MoA

Uses

Toxicity

Antiandrogen
Inhibits steroid binding
Treats PCOS to prevent hirsutism
Tox: gynecomastia and amenorrhea

Estrogens

Names

MoA

Use

Tox

Contraindication

Ethinly, Estradiol, DES, Mestranol
Binds Estrogen receptors
Treats Hypogonadism or Ovarian Failure, Menstrual abnormalities, HRT in postmenop...

Names of Selective Estrogen Receptor Modulators (SERMs)


Clomiphene, Tamoxifen, Raloxifene


Clomiphene

Kind of Drug

MoA

Uses

Toxicity

SERM
Partial agonist at estrogen receptors in hypothalamus. Prevents normal feedback inhibition and ↑ LH and FSH from pituitary.
Treats infer...

Tamoxifen
Kind of Drug
MoA
Uses

SERM
Antagonist of estrogen receptors in breast tissue
Treats and prevents recurrence of ER+ breast cancer

Related Flashcard Decks

Study Tips

  • Press F to enter focus mode for distraction-free studying
  • Review cards regularly to improve retention
  • Try to recall the answer before flipping the card
  • Share this deck with friends to study together
TermDefinition

Ketoconazole

Kind of drug

MoA

Uses

Toxicity

Antiandrogen
Inhibits steroid synthesis (--/ 17,20 desmolase)
Treats PCOS to prevent hirsutism
Tox: gynecomastia and amenorrhea

Spironolactone

Kind of drug

MoA

Uses

Toxicity

Antiandrogen
Inhibits steroid binding
Treats PCOS to prevent hirsutism
Tox: gynecomastia and amenorrhea

Estrogens

Names

MoA

Use

Tox

Contraindication

Ethinly, Estradiol, DES, Mestranol
Binds Estrogen receptors
Treats Hypogonadism or Ovarian Failure, Menstrual abnormalities, HRT in postmenopausal women
Used in men to treat androgen dependent prostate cancer
Tox: ↑ risk of endometrial cancer, bleeding in postmenopausal women, clear cell carcinoma of the vagina/cervix in females exposed to DES in utero, ↑ risk of thrombi
ER+ breast cancer, history of DVTs

Names of Selective Estrogen Receptor Modulators (SERMs)


Clomiphene, Tamoxifen, Raloxifene


Clomiphene

Kind of Drug

MoA

Uses

Toxicity

SERM
Partial agonist at estrogen receptors in hypothalamus. Prevents normal feedback inhibition and ↑ LH and FSH from pituitary.
Treats infertility and PCOS
Tox: Hot flashes, ovarian enlargement, multiple simultaneous pregnancies, visual disturbances

Tamoxifen
Kind of Drug
MoA
Uses

SERM
Antagonist of estrogen receptors in breast tissue
Treats and prevents recurrence of ER+ breast cancer

Raloxifene
Kind of Drug
MoA
Uses

SERM
Agonist of estrogen receptors in bone and reduces bone resorption
Treats osteoporosis

Hormone Replacement Therapy
Uses
Toxicity

Used for the relief or prevention of menopausal symptoms (hot flashes, vaginal atrophy, etc) and osteoporosis (by ↑ estrogen --> ↓ osteoclast activity)
Unopposed use of estrogen --> ↑ risk of endometrial cancer, so progesterone is added. Possible ↑ CV risk

Anastrozole/Exemestane
MoA
Uses

Aromatase inhibitor used to treat postmenopausal women with breast cancer

Progestins
MoA
Uses

Binds progesterone receptors. Reduces growth and ↑ vascularization of endometrium
Used in oral contraceptives and treatment of endometrial cancer and abnormal uterine bleeding

Mifepristone (RU-486)

MoA

Co-administered with...

Use

Tox

Competitive inhibitor of progestins at progesterone receptor
Termination of pregnancy. Administered w/ misoprostol (PGE)
Tox: Heavy bleeding, GI effects (nausea, vomiting, anorexia), Abdominal pain

Oral Contraception
What does it consist of?
MoA
Contraindications

Progestins + Estrogen
E and P --/ LH/FSH which leads to prevention of estrogen surge. No estrogen surge --> no LH surge. No LH surge --> no ovulation
Progestins cause thickening of the cervical mucus, thereby limiting access of sperm to uterus.
Progestins --/ endometrial proliferation making it less suitable for implantation
Contraindicated in smokers >35 (CV events), Hx of Thromboembolism and stroke or Hx of estrogen dependent tumors

Terbutaline
MoA
Uses

β2 agonist that relaxes uterus

| Reduces premature uterine contractions

Tamsulosin
MoA
Uses
Selectivity

α1 antagonist used to treat BPH by inhibiting smooth muscle contraction
Selective for α1A and α1D (on prostate) vs α1B (vasculature)

Sildenafil, Vardenafil

MoA

Uses

Tox

Contraindications

--/ Phosphodiesterase 5 causing an ↑ in cGMP, smooth muscle relaxation in corpus cavernosum, ↑ blood flow, and penile erection
Treats erectile dysfunction
Tox: "Hot and sweaty, but then Headache , Heartburn, Hypotension"
Headache, flushing, dyspnea, impaired blue-green color vision, Hypotension
Risk of life threatening hypotension in nitrate users

Danazol
MoA
Uses
Tox

Synthetic androgen that is a partial agonist at androgen receptor
Endometriosis and hereditary angioedema
Wt Gain, Edema, Acne, Hirsutism, Masculinization, ↓HDL, Hepatotoxicity

Endometriosis

What is it?

What tissue is affected?

What does it cause?

What causes it?

Non-neoplastic endometrial glands/stroma in abnormal locations

In Ovary or on Peritoneum

Cyclic bleeding (menstrual type) resulting in blood filled "chocolate cysts"

Caused by retrograde menstrual flow

Endometriosis

Clinical manifestation?

Treatment

Dysmenorrhea, Menorrhagia, Dyspareunia, Infertility
Uterus is normal size
Treat with oral contraceptives, NSAIDs, Leuprolide, Danazol

Adenomyosis
What is it?
Clinical manifestation
Treatment

Endometrium within myometrium
Menorrhagia, Dysmenorrhea, Pelvic pain
Enlarged uterus
Hysterectomy

Cervical Dysplasia and Carcinoma In Situ

Description

Where does it begin and extend?

Classification

Histology

Disordered epithelial growth
Begins at basal layer of squamo-columnar junction and extends outwards
CIN1, CIN2, CIN3 (severe dysplasia or carcinoma in situ) depending on how high the basal cells extend
Koilocytes: raisinoid nuclei with perinuclear halo

Cervical Dysplasia and Carcinoma In Situ

Viral cause?

Mechanism of viral cause?

Prevention?

Risk if untreated

Risk factors

HPV16 and HPV18 (E6 --/ p53 andE7 --/ RB)
Vaccine available
May progress to invasive carcinoma if left untreated
Multiple sexual partners, smoking , early intercourse, HIV

Cervical Invasive Carcinoma
Most often what kind of carcinoma?
Screen?
Complications

Often squamous cell carcinoma
Pap smear
Lateral invasion can block ureter leading to renal failure

PCOS

PathoPhys

Gross

Clinical manifestation

Associated w/

Increased risk for

↑ frequency of pulsatile GnRA release --> ↑LH + ↓FSH --> anovulation --> no progesterone
Hyperandrogenism b/c of deranged steroid synthesis by Theca cells
Bilaterally enlarged, cystic ovaries
Amenorrhea, infertility, obesity, hirsutism
Associated with insulin resistance
Risk for endometrial cancer (↑ estrogen + no progesterone to oppose --> ↑ aromatization of testosterone in fat)

PCOS treatment

Wt reduction
Low does Oral Contraceptive or medroxyprogesterone (↓ LH and androgenesis)
Spironolactone (acne and hirsutism)
Clomiphene (infertility)
Meformin (diabetes or metabolic syndrome)

Endometrial hyperplasia

What is it?

What causes it?

Increased risk for...

Presentation

Risk factors

Abnormal endometrial gland proliferation

Caused by excess estrogen stimulation

↑ risk for endometrial carcinoma

Postmenopausal vaginal bleeding

Anovulatory cycle, HRT, PCOS, Granulosa Cell Tumor

Endometrial Carcinoma

Frequency

Epidemiology

Presentation

Typically preceded by

Risk factors

Prognosis

Most common gynecologic malignancy
Peak occurrence at 55-65
Vaginal bleeding
Typically preceded by endometrial hyperplasia
Prolonged use of estrogen w/o progesterone, obesity, diabetes, HTN, nulliparity, late menopause
↑ myometrial invasion --> poor prognosis

Types of Myometrial tumors

Leiomyoma (fibroid)

| Leiomyosarcoma

Leiomyoma

Type of tumor

Frequency

Gross

Epidemiology

What kind of tissue

Malignant?

Myometrial tumor
Most common of all tumors in females
Multiple tumors with well-demarcated borders
↑ incidence in blacks. Peak at 20-40
Benign smooth muscle tumor
Malignant transformation to Leiomyosarcoma is rare

Leiomyoma

Hormone sensitive?

Presentation

Complications

Histology

Estrogen sensitive: tumor size ↑ w/ pregnancy and ↓ w/ menopause
May be asymptomatic, cause abnormal uterine bleeding, miscarriage
Severe bleeding may lead to Iron Deficiency Anemia
Whorled pattern of smooth muscle fibers

Leiomyosarcoma

Kind of tumor

Gross

Where does it arise from?

Epidemiology

Prognosis

Myometrial tumors

Bulky, irregular shaped tumor with areas of necrosis and hemorrhage. May protrude from cervix and bleed

Typically arising de novo

↑ incidence in middle aged black women

Highly aggressive w/ tendency to recur

Hydatidiform Moles

What are they?

Types

Presentation

Precursor of...

Serum marker

Gross

Potential complication

Treatment

Cystic swelling of chorionic villi and proliferation of chorionic epithelium (trophoblast)

Complete vs Partial

Presents with abnormal vaginal bleeding

Most common precursor of choriocarcinoma

↑βhCG

Honeycomb uterus or cluster of grapes appearance. Enlarged uterus

Uterine rupture

dilation and curettage and methotrexate

Complete Hydatidiform moles

Appearance

Fetus?

Karyotype

hCG

Uterine size

Conversion to choriocarcinoma

Fetal parts

Components

Risk of complications

Snowstorm appearance with no fetus during 1st sonogram

46XX, 46XY

↑↑↑↑ hCG

↑ uterine size

2% choriocarcinoma

No fetal parts

2 sperm (from same sperm that replicated) + empty egg

15-20% malignant trophoblastic disease

Partial Hydatidiform moles

Karyotype

hCG

Uterine size

Conversion to choriocarcinoma

Fetal parts

Components

Risk of complications

69XXX, 69XXY, 69XYY

↑ hCG

No change in uterine size

Rare choriocarcinoma

Has fetal parts

2 sperm + 1 egg

Low risk of malignancy

Classical Preeclampsia presentation

Pregnant women with HTN, Proteinuria, and Edema

Classical Presentation of Eclampsia

Preeclampsia + Seizures

Preeclampsia

Frequency

When

↑ risk in...

Caused by

Associated w/

Mortality results from

7% of pregnant women from 20 weeks to 6 weeks postpartum
↑ risk in pts w/ HTN, Diabetes, Chronic Renal Disease, Autoimmune disorders
Impaired vasodilation of spiral arteries --> Placental ischemia --> ↑ vascular tone
Associated with HELLP syndrome
Death from cerebral hemorrhage and ARDS

HELLP Syndrome


Hemolysis, Elevated Liver enzymes, Low Platelets


Clinical Manifestations of Preeclampsia

| Lab findings

Headache, Blurred vision, Abdominal pain, Edema of face and extremities, altered mentation, hyperreflexia
Thrombocytopenia and Hyperuricemia

Treatment Preeclampsia

Delivery of fetus as soon as possible, Bed rest, monitoring, treat HTN
IV MgSulfate to prevent seizures

Ovarian germ cell tumors most common in…

Adolescents

Dysgerminoma

What kind of tumor?

Malignant?

Equivalent in male?

Histology

Associated w/

Markers

Ovarian germ cell tumor

Malignant

Equivalent to male seminoma but rarer (1% over 30%)

Sheets of uniform cells

Associated with Turners Syndrome

hCG and LDH

Choriocarcinoma in females

What kind of tumor?

Frequency

Malignant

Who develops it?

When does it develop?

Source

Histology

What other pathologies is it related to?

Metastases

Serum markers

Ovarian germ cell tumor

Rare but malignant

Develops during or after pregnancy in mother or baby

From trophoblastic tissue

No chorionic villi and ↑ theca-lutein cysts

On spectrum with moles as gestational trophoblastic neoplasms

Early homogenous spread to lungs

hCG

Yolk Sac (Endodermal Sinus) Tumor in women

What kind of tumor?

Malignant?

Location

What kind of pt?

Gross

Histology

Marker

Ovarian germ cell tumor

Aggressive malignancy in ovaries/testes and sacrococcygeal area of young children

Yellow, friable, solid masses

50% of Schiller-Duval bodies (resemble glomeruli)

AFP

Teratoma in women

What kind of tumor

Frequency

Types of tissue?

Types

Ovarian germ cell tumor

90% of ovarian germ cell tumors

Contains cells from 2 or 3 germ layers

Mature vs. Immature

Mature Teratoma in women
Gross
Frequency
Malignant?

Dermoid Cyst
Most common ovarian germ cell tumor
Mostly benign

Immature Teratoma in women
Malignant?
Gross
Presentation

Aggressively malignant
Can have Struma Ovarii (functional thyroid tissue)
Can present as hyperthyroidism

Serous Cystadenoma

Kind of tumor

Frequency

Distribution

Histology

Malignant?

Ovarian non-germ cell tumor

45% of ovarian tumors

Bilateral

Lined with fallopian tube-like epithelium

Benign

Marker for Ovarian cancer?

↑ CA-125

| Good for monitoring progression but not screening

Serous cystadenocarcinoma

Kind of tumor

Frequency

Distribution

Histology

Malignant?

Genetic risk factors

Ovarian non-germ cell tumor

45% of ovarian tumors

Bilateral

Psammoma bodies

Malignant

BRCA1, BRCA2, HNPCC

Mucinous Cystadenoma
Kind of tumor
Malignant
Histology

Ovarian non-germ cell tumor
Benign
Multilocular cyst lined by mucus secreting epithelium. Intestine-like tissue

Mucinous Cystadenocarcinoma
Kind of tumor
Malignant?
Complication

Ovarian non-germ cell tumor
Malignant
Pseudomyxoma peritonei - intraperitoneal accumulation of mucinous material from ovarian or appendiceal tumor

Brenner Tumor

Kind of tumor

Malignant

Distribution

Gross

Histology

Ovarian non-germ cell tumor

Benign

Unilateral

Looks like Bladder. Solid tumor that is pale yellow-tan color and appears encapsulated

Coffee bean nuclei on H&E

Fibromas

Kind of tumor?

Histology

Complication

Clinical Manifestation

Ovarian non-germ cell tumor
Bundles of spindle shaped fibroblasts
Meigs' Syndrome
Pulling sensation in groin

Meigs Syndrome

Ovarian fibroma + ascites + hydrothorax

Granulosa Cell Tumor

What kind of tumor

Hormones

Complications in kids vs adults

Histology

Presentation

Granulosa Cell Tumor

What kind of tumor

Hormones

Complications in kids vs adults

Histology

Presentation

Krukenberg Tumors
Kind of tumor
Source
Histology

Ovarian non-germ cell tumor
GI malignancy that metastasizes to ovaries
Mucin secreting signet cell adenocarcinoma

Squamous Cell Carcinoma of the Vagina Usually secondary to…


SCC of cervix


Women at risk for Clear Cell Adenocarcinoma of the Vagina


DES exposure in utero


Sarcoma Botryoides (rhabdomyosarcoma variant)
Kind of tumor
Classic pt
Histology

Vaginal Tumor
Girls <4
Spindle shaped, Desmin+ tumor cells

Dizygotic twins

Frequency

Egg #

Amniotic sacs

Placentas

80% of twins
2 eggs
2 separate amniotic sacs
2 separate placentas (chorions)

Monozygotic twins that split day 0-4

Stage

Frequency

Placenta

Amniotic sacs

Chorion

Morula

25%

Fused or separate placenta

Diamniotic

Dichorionic

Monozygotic twins that split day 4-8

Stage

Frequency

Amniotic sacs

Chorion

Blastocyst
75%
Diamniotic
Monochorionic

Monozygotic twins that split day 8-12
Frequency
Amniotic sacs
Chorion

Less than 1%
Monoamniotic
Monochorionic

Monozygotic twins that split after day 13

Monoamniotic
Monochorionic
Conjoined

Fetal Components of the placenta

Cytotrophoblast and Syncytiotrophoblast

Cytotrophoblast
Where is it?
What is it made from?
Where is it from?

Inner layer of chorionic villi
Cytotrophoblast made from Cells
Fetal component

Syncytiotrophoblast
Where is it?
What does it secrete?

Outer layer of chorionic villi

| Secretes hCG

Maternal component of placenta
Name
Derived from?

Decidua Basalis

| Derived from endometrium

Where is maternal blood in the placenta?


In Lacunae


What makes up the Umbilical Cord?


2 Umbilical arteries and 1 Umbilical vein


Function of umbilical arteries

| Source?

Return deoxygenated blood from fetal internal iliac arteries to placenta


Function of umbilical vein?

| What does it drain into?

Supplies oxygenated blood from placenta to fetus

| Drains via ductus venosus into IVC

Single umbilical artery is associated with…

Congenital and Chromosomal Anomalies

What are the umbilical arteries and veins are derived from?


The Allantois


Urachal Duct
What is it?
Development?
Failure to obliterate?

A duct between bladder and yolk sac
3rd week: Yolk sac forms allantois which extends into urogenital sinus. Allantois becomes urachus
Patent Urachus: urine discharge from the umbilicus
Vesicourachal diverticulum: outpouching of bladder

Vitelline duct

Name

Function

When is it obliterated

Failure to obliterate

Omphalo-Mesenteric Duct
Connects yolk sac to midgut lumen
Obliterated at week 7
Vitelline fistula: meconium discharge from umbilicus
Meckel's Diverticulum: Ectopic gastric and pancreatic tissue --> melena, periumbilical pain, ulcer

1st Aortic Arch forms


Maxillary artery (branch of external carotid)


2nd Aortic Arch forms


Stapedial artery and Hyoid artery


3rd Aortic Arch forms


Common Carotid artery and proximal part of Internal Carotid artery


4th Aortic Arch forms


L: Aortic arch
R: Proximal part of Subclavian artery

6th Aortic Arch forms


Proximal part of pulmonary arteries and (on left only) ductus arteriosus


Branchial Apparatus
AKA
Composition with origin

Pharyngeal Apparatus

"CAP"

Clefts (grooves) from Ectoderm

Arches from Mesoderm (muscles, arteries) and neural crest cells (bones, cartilage)

Pouches from Endoderm

Branchial Clefts develop into

1st: External auditory meatus

| 2nd - 4th: form temporary cervical sinus which are obliterated by proliferation of 2nd arch mesenchyme

Persistent Cervical Sinus

Branchial cleft cyst within lateral neck

1st Branchial Arch

Cartilage

Muscles

Nerves

Pathology

Meckel's cartilage: Mandible, Malleus, incus, spheno-Mandibular ligament
Muscles of Mastication (Temporalis, Masseter, Lat and Med Pterygoids), Mylohyoid, Anterior belly of the digastric, Tensor Tympani, Tensor Veli Palatini
V2 and V3
Treacher Collins Syndrome --> 1st arch crest fails to migrate --> Mandibular hypoplasia and facial abnormalities

2nd Branchial Arch
Cartilage
Muscles
Nerves

Reichert's Cartilage (Stapes, Styloid Process, Lesser horn of the Hyoid, Stylohyoid ligament)
Muscles of facial expression, Stapedius, Stylohyoid, Posterior Belly of the Digastric
CNVII

3rd Branchial Arch

Cartilage

Muscles

Nerves

Pathology

Greater horn of hyoid
Stylopharyngeus
CN IX ("swallow stylishly")
Congenital Pharyngo-Cutaneous Fistula: Persistence of cleft and pouch --> Fistula between tonsillar area, cleft in lateral neck

4th - 6th Branchial Arch
Cartilage
Muscles
Nerves

Thyroid, Cricoid, Arytenoids, Corniculate, Cuneiform
4th: Most Pharyngeal Constrictors; Cricothyroid, Levator Veli Palatini
6th: All intrinsic muscles of larynx except cricothyroid
CNX: 4th is superior laryngeal branch ("simply swallow"), 6th is recurrent laryngeal branch ("speak")

Branchial Arches Mnemonic

Chew, Smile, Swallow Stylishly, Simply Swallow, Speak

What forms posterior 1/3 of tongue

Branchia Arches 3 and 4

What does Branchia Arch 5 become?

5 makes no major developmental contributions

1st Branchial Pouch
Develops into
What does it contribute to?

Middle Ear Cavity, Eustachian Tube, Mastoid Air Cells

| Contributes to Endoderm-lined structures of ear

2nd Branchial Pouch develops into…

Epithelial lining of palatine tonsil

3rd Branchial pouch
Develops into…
Where does it end up

Dorsal wings develop into inferior parathyroids
Ventral wing develops into Thymus
Ends up below 4th

4th Branchial pouch develops into…

Dorsal wings develop into superior parathyroids

DiGeorge Syndrome
What develops abnormally
PathoPhys

Aberrant development of 3rd and 4th Branchial pouches

| T cell deficiency (Thymic aplasia) and Hypocalcemia (parathyroid doesn't develop)

Cleft Lip

Failure of fusion of maxillary and Medial Nasal Processes (formation of primary palate)

Cleft Palate

Failure of fusion of the lateral palatine processes, the nasal septum, and/or the median palatine process (formation of secondary palate)

Cleft Lip vs Cleft Palate

2 distinct etiologies but often occur together

Female genital development
What kind of pathway?
Ducts?

Default pathway

| Mesonephric duct degenerates and Paramesonephric duct develops