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COMLEX Level 1 TrueLearn COMBank - Questions Answered With Expert Insights

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COMLEX Level 1 TrueLearn COMBank - Questions Answered With Expert Insights

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Geüpload op
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Aantal pagina's
105
Geschreven in
2024/2025
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COMLEX Level 1 TrueLearn COMBank - Questions
Answered With Expert Insights
Failure to deliver the placenta within 30 mins of birth

Manual extraction may result in profuse, uncontrollable bleeding,
w/ retention of most or all of the placental tissue

Emergent hysterectomy is required

Placental villi attach to the surface of the myometrium Correct
Answer - Placenta accreta

What are the risk factors of placental accreta spectrum Correct
Answer - Hx of c-section
Hx of uterine procedures (dilation, curettage, myomectomy, uterine
ablation, Asherman syndrome)
Placental previa

What is included in placenta accreta spectrum and describe each
Correct Answer - Placenta accreta: placental villi attach to the
surface of the myometrium

Placenta increta: chorionic villi penetrate into the myometrium

Placenta precreta: chorionic villi penetrate through the
myometrium to the uterine serosa or adjacent organs

Secondary amenorrhea (absence of periods for 3 cycles) following a
dilation and curettage (D&C) Correct Answer - Asherman
syndrome

,- Trauma to stratum basalis --> absence of the stratum basalis layer
of the endometrium

Etiology of secondary amenorrhea Correct Answer -
Hypothalamic: Functional hypothalamic amenorrhea

Pituitary: Hyperprolactinemia, empty sella syndrome, Sheehan
syndrome

Ovary: Plycystic ovary syndrome, premature ovarian failure

Uterus: Asherman syndrome

Other: Congenital adrenal hyperplasia, hypothyroidism, adrenal
tumors

List the disease for each histology:
1. Abscent stratum basalis in an endometrial biopsy
2. Benign keratinocytes within the epidermis
3. Enlarged ovaries w/ multiple cystic follicles
4. Hyperplasia of lactotroph cells within the anterior pituitary
5. Numerous corpora albicans and a fibrotic cortex Correct
Answer - 1. Asherman syndrome
2. Imperforate hymen
3. Polycystic ovary syndrome
4. Prolactinoma
5. Atrophic ovary

Diagnosed in infants (< 1 year)

M > F predominance

Most common in Caucasian populations

,Symptoms of severe anemia --> pallor, fatigue, cyanosis

Webbed neck (can be confused for Turner syndrome)

Cleft pallet

Triphalangeal thumbs

Macrocytic anemia (nonmegaloblastic)

Decreased reticulocyte count (< 1% in infants)

Normal leukocytes and platelets

Bone marrow biopsy --> absence of erythroid precursors

Increased HbF on electrophoresis

Nonmegaloblastic macrocytic anemia Correct Answer -
Diamond-Blackfan anemia

- Turner syndrome does not cause macrocytic anemia

Treatment for Diamond-Blackfan anemia Correct Answer -
Corticosteroids
Transfusion
Hematopoietic stem cell transplant

Defect in erythropoiesis --> Pure Red Cell Aplasia (PRCA)

Erythroblasts in bone marrow undergo premature apoptosis

, Common mutations result in ribosome protein synthesis defect -->
TP53 activation --> increased apoptosis Correct Answer -
Diamond-Blackfan anemia

Megaloblastic macrocytic anemias (3) Correct Answer - B12
deficiency
Folate deficiency
Orotic aciduria

Nonmegaloblastic macrocytic anemias (4) Correct Answer -
Diamond-Blackfan anemia
Alcohol use
Liver disease
Thyroid disease

Normocytic anemia

Maybe due to: viral infections (eg., parvovirus), radiation,
medications (eg, antimetabolites), and toxin exposure

Pncytopenia (anemia, thrombocytopenia, leukopenia) Correct
Answer - Aplastic anemia

Autosomal recessive

Defect in DNA repair mechanisms

Either normocytic or macrocytic anemia

Pancytopenia (labs show anemia, thrombocytopenia, leukopenia)
Correct Answer - Fanconi anemia

Autosomal recessive
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