COMLEX Level 1 Placenta Accreta Quiz
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Questions and Answers

What is failure to deliver the placenta within 30 minutes of birth called?

Placenta accreta

What are the risk factors of placental accreta spectrum?

History of c-section, history of uterine procedures, placental previa

What are the types of placenta accreta spectrum?

Placenta accreta, placenta increta, placenta percreta

What condition is characterized by secondary amenorrhea following a D&C?

<p>Asherman syndrome</p> Signup and view all the answers

What are the causes of secondary amenorrhea?

<p>Hypothalamic, pituitary, ovarian, uterine, and other causes</p> Signup and view all the answers

Match the disease with its corresponding histology:

<p>Abscent stratum basalis in an endometrial biopsy = Asherman syndrome Benign keratinocytes within the epidermis = Imperforate hymen Enlarged ovaries with multiple cystic follicles = Polycystic ovary syndrome Hyperplasia of lactotroph cells within the anterior pituitary = Prolactinoma Numerous corpora albicans and a fibrotic cortex = Atrophic ovary</p> Signup and view all the answers

What is characterized by severe anemia in infants with symptoms such as webbed neck and macrocytic anemia?

<p>Diamond-Blackfan anemia</p> Signup and view all the answers

What is the treatment for Diamond-Blackfan anemia?

<p>Corticosteroids, transfusion, hematopoietic stem cell transplant</p> Signup and view all the answers

What defect leads to Diamond-Blackfan anemia?

<p>Defect in erythropoiesis</p> Signup and view all the answers

List three causes of megaloblastic macrocytic anemias.

<p>B12 deficiency, folate deficiency, orotic aciduria</p> Signup and view all the answers

List four causes of nonmegaloblastic macrocytic anemias.

<p>Diamond-Blackfan anemia, alcohol use, liver disease, thyroid disease</p> Signup and view all the answers

What is a common cause of normocytic anemia in young children?

<p>Aplastic anemia</p> Signup and view all the answers

What condition is characterized by an autosomal recessive defect in DNA repair mechanisms?

<p>Fanconi anemia</p> Signup and view all the answers

What results from a defect in uridine monophosphate synthase and causes megaloblastic macrocytic anemia?

<p>Orotic aciduria</p> Signup and view all the answers

What causes megaloblastic macrocytic anemia with hypersegmented neutrophils?

<p>Vitamin B12 deficiency</p> Signup and view all the answers

What are common causes of macrocytic anemia in young children?

<p>Orotic aciduria, Diamond-Blackfan anemia</p> Signup and view all the answers

What conditions are associated with microcytic anemia in young children?

<p>Lead poisoning, sideroblastic anemia, thalassemias</p> Signup and view all the answers

What are some causes of normocytic anemia in young children?

<p>Aplastic anemia, hereditary spherocytosis, leukemia</p> Signup and view all the answers

Study Notes

Placenta Accreta

  • Defined as failure to deliver the placenta within 30 minutes of birth, leading to potential complications.
  • Manual extraction can cause uncontrollable bleeding and retention of placental tissue.
  • Emergent hysterectomy may be necessary due to severe hemorrhaging.
  • The condition involves placental villi attaching to the myometrium surface.

Risk Factors for Placenta Accreta Spectrum

  • History of cesarean section (c-section) increases risk.
  • Previous uterine procedures, including dilation, curettage, myomectomy, and uterine ablation, are significant factors.
  • Presence of placental previa also raises the likelihood of developing this spectrum.

Placenta Accreta Spectrum Components

  • Placenta Accreta: Villi attach superficially to the myometrium.
  • Placenta Increta: Villi penetrate deeper into the myometrium.
  • Placenta Precreta: Villi invade through the myometrium to the uterine serosa or surrounding organs.

Asherman Syndrome

  • Characterized by secondary amenorrhea after dilation and curettage (D&C).
  • Results from trauma to the stratum basalis, leading to its absence in the endometrium.

Etiology of Secondary Amenorrhea

  • Hypothalamic issues: Functional hypothalamic amenorrhea.
  • Pituitary causes: Hyperprolactinemia, empty sella syndrome, and Sheehan syndrome.
  • Ovarian disorders: Polycystic ovary syndrome and premature ovarian failure.
  • Uterine condition: Asherman syndrome.
  • Other contributing factors include congenital adrenal hyperplasia, hypothyroidism, and adrenal tumors.

Histology and Associated Diseases

  • Absent stratum basalis: Asherman syndrome.
  • Benign keratinocytes: Indicative of imperforate hymen.
  • Enlarged ovaries: Found in polycystic ovary syndrome.
  • Hyperplasia of lactotroph cells: Seen in prolactinoma.
  • Corpora albicans and fibrotic cortex: Suggests atrophic ovary.

Diamond-Blackfan Anemia

  • Diagnosed in infants with a male predominance.
  • Most prevalent in Caucasian populations, presenting with symptoms of anemia like pallor and fatigue.
  • Notable features include webbed neck, cleft palate, and triphalangeal thumbs.
  • Associated with macrocytic anemia that is nonmegaloblastic, showing decreased reticulocyte count and normal leukocytes and platelets.
  • Bone marrow biopsy demonstrates absence of erythroid precursors.

Treatment Options for Diamond-Blackfan Anemia

  • Corticosteroids are standard treatment.
  • Blood transfusions may be necessary.
  • Hematopoietic stem cell transplant can be indicated.

Pure Red Cell Aplasia (PRCA)

  • Associated with defects in erythropoiesis leading to Diamond-Blackfan anemia.
  • Bone marrow erythroblasts undergo premature apoptosis due to mutations affecting ribosomal protein synthesis, resulting in TP53 activation.

Types of Macrocytic Anemia

  • Megaloblastic: Includes B12 deficiency, folate deficiency, and orotic aciduria.
  • Nonmegaloblastic: Includes Diamond-Blackfan anemia, alcohol use, liver disease, and thyroid disease.

Aplastic Anemia

  • Characterized as normocytic anemia potentially due to viral infections, radiation, medications, or toxins.
  • Presents with pancytopenia, including anemia, thrombocytopenia, and leukopenia.

Fanconi Anemia

  • An autosomal recessive disorder involving DNA repair defects.
  • Can present with either normocytic or macrocytic anemia and also causes pancytopenia.

Orotic Aciduria

  • Another autosomal recessive condition with a defect in UMP synthase leading to elevated orotic acid and failure to thrive.
  • Presents with delayed development and megaloblastic macrocytic anemia unresponsive to folate and B12 supplementation.

Vitamin B12 Deficiency Anemia

  • Results in megaloblastic macrocytic anemia with the presence of hypersegmented neutrophils.
  • Causes include a vegan diet, pernicious anemia, gastrectomy, gastric bypass, and ileal diseases such as Crohn's.

Anemia in Young Children

  • Microcytic Anemias: Lead poisoning, sideroblastic anemia, thalassemias.
  • Normocytic Anemias: Aplastic anemia, hereditary spherocytosis, leukemia, microangiopathic hemolytic anemia, pyruvate kinase deficiency, Rh incompatibility, sickle-cell anemia.
  • Macrocytic Anemias: Orotic aciduria and Diamond-Blackfan anemia.

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Description

Test your knowledge on placenta accreta and its related risk factors with this quiz designed for COMLEX Level 1 preparation. Understand the critical definitions and implications of failure to deliver the placenta. Prepare effectively for your medical exams!

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