WBR0345
Author | [[PageAuthor::Rim Halaby, M.D. [1] (Reviewed by Alison Leibowitz)]] |
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Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Pathophysiology |
Sub Category | SubCategory::Hematology |
Prompt | [[Prompt::A 2-year-old male is brought by his mother to the physician's office for delayed speech. The mother informs you that, unlike his older siblings at his age, the patient is irritable and hyperactive. Further questioning reveals that the patient's family lives in an old house with chipped paint. Physical examination is remarkable for pallor. Complete blood count (CBC) demonstrates hemoglobin levels of 9.8 g/dL and MCV: 68 fl. A peripheral smear of the patient's blood displays basophilic stippling. Based on the simplified diagram of heme synthesis shown below, which of the following steps is most likely inhibited in this patient? |
Answer A | AnswerA::A |
Answer A Explanation | AnswerAExp::"A" corresponds to ALA-synthase, inhibited by B6 deficiency and in hereditary conditions, such as X-linked ALA-synthase deficiency. |
Answer B | AnswerB::B |
Answer B Explanation | AnswerBExp::See explanation. |
Answer C | AnswerC::C |
Answer C Explanation | AnswerCExp::"C" corresponds to porphobilinogen deaminase. Deficiency of this enzyme typically causes acute intermittent porphyria. |
Answer D | AnswerD::D |
Answer D Explanation | [[AnswerDExp::"D" corresponds to uroporphyrinogen III synthase. Uroporphyrinogen III synthase deficiency is associated with Gunther's disease.]] |
Answer E | AnswerE:: |
Answer E Explanation | AnswerEExp::"E" corresponds to uroporphyrinogen decarboxylase, which is typically deficient in porphyria cutanea tarda. |
Right Answer | RightAnswer::B |
Explanation | [[Explanation::The patient in this scenario most likely has lead poisoning secondary to chronic exposure to lead-based paint flakes in the old residency. Other environmental or occupational sources of lead are from the manufacturing or recycling of automobile batteries, lead smelting plant, lead-containing gasoline, and moonshine whiskey made in lead stills.
Lead is readily absorbed through the respiratory tract and incorporated into the bone, where it competes with calcium and causes impaired remodeling of cartilage and trabecular bone in the epiphyses, which is detected as radiodense lead lines. Central nervous system disturbances, manifesting as loss of short-term memory, delayed development, behavioral changes, or hearing impairment, are more common in children due to the relatively permeable blood-brain barrier, whereas demyelinating peripheral neuropathies predominate in adult patients. Additional findings of lead intoxication include abdominal pain, tubulointerstitial nephritis, and microcytic hypochromic anemia. Basophilic stippling, which represents precipitated ribosomes in reticulocytes, may be evident on the peripheral blood film. A definitive diagnosis is established with the detection of elevated serum levels of lead and protoporphyrin. Anemia, in chronic lead poisoning, entails the blockade of several enzymes including pyrimidine-5'-nucleotidase-1 (P5'N-1), ferrochelatase, and 5-aminolevulinate (ALA) dehydratase. Inhibition of P5'N-1 interrupts the hydrolysis of uridine monophosphate (UMP) and cytidine monophosphate (CMP) resulting in the reduced availability of nucleosides, which in turn leads to ineffective hematopoiesis and accelerated turnover. In the heme biosynthesis pathway, lead inhibits the activity of ALA dehydratase, which converts ALA into porphobilinogen in the cytoplasm, and ferrochelatase, which incorporates the ferrous iron into protoporphyrin IX in the mitochondria. Anemia associated with chronic lead poisoning is typically microcytic and hypochromic. |
Approved | Approved::Yes |
Keyword | WBRKeyword::lead poisoning, WBRKeyword::lead toxicity, WBRKeyword::ALA dehydratase, WBRKeyword::ferrochelatase, WBRKeyword::anemia, WBRKeyword::microcytic, WBRKeyword::hypochromic, WBRKeyword::basophilic stippling |
Linked Question | Linked:: |
Order in Linked Questions | LinkedOrder:: |