Soru

Zorluk: ZorOrdering Laboratory Tests

Match each patient's clinical presentation with the most appropriate targeted laboratory test to confirm the underlying etiology or assess disease-specific risk.

  • A 35-year-old woman with a history of recurrent late-term pregnancy losses presenting with a prolonged activated partial thromboplastin time that fails to correct with a normal plasma mixing study.Dilute Russell viper venom time (dRVVT)
  • A 52-year-old man presenting with chronic, destructive sinusitis, cavitary pulmonary lesions on chest imaging, and acute kidney injury with red blood cell casts.Proteinase-3 antineutrophil cytoplasmic antibody (PR3-ANCA) assay
  • A 45-year-old woman with rapidly progressive skin thickening over her trunk and proximal extremities presenting with acute oliguric renal failure and a blood pressure of 210/118 mmHg.Anti-RNA polymerase III antibody testing
  • A 62-year-old woman evaluated for an acute onset of proximal muscle weakness and a violaceous periorbital rash, who was recently found to have a malignant ovarian mass.Anti-transcriptional intermediary factor 1-gamma (anti-TIF1-γ) antibody assay

Cevap

Match the prolonged uncorrectable aPTT with dRVVT; the destructive sinusitis and glomerulonephritis with PR3-ANCA; the scleroderma renal crisis with Anti-RNA polymerase III; and the paraneoplastic dermatomyositis with Anti-TIF1-γ.
Each clinical vignette represents a specific autoimmune or rheumatologic syndrome that requires a highly targeted laboratory test for definitive diagnosis or risk stratification. Dilute Russell viper venom time (dRVVT) confirms lupus anticoagulant in antiphospholipid syndrome. PR3-ANCA is highly sensitive and specific for granulomatosis with polyangiitis. Anti-RNA polymerase III is a major risk factor for scleroderma renal crisis in systemic sclerosis. Anti-TIF1-γ is a specific marker for paraneoplastic dermatomyositis.

Adım Adım Çözüm

1
Analyze the first presentation (recurrent fetal loss, uncorrectable aPTT).
Identify suspected Antiphospholipid Syndrome (APS) secondary to lupus anticoagulant.
Mixing study failure indicates an inhibitor. Recurrent miscarriages paired with this lab anomaly are classic for APS, which is confirmed using a dilute Russell viper venom time (dRVVT) assay.
2
Analyze the second presentation (destructive sinusitis, cavitary lung lesions, nephritic syndrome).
Identify suspected granulomatosis with polyangiitis (GPA).
This specific multi-organ involvement (upper airway, lower airway, and kidneys) requires PR3-ANCA testing for diagnostic confirmation.
3
Analyze the third presentation (rapid skin thickening, malignant hypertension, acute kidney injury).
Identify scleroderma renal crisis (SRC).
SRC is a life-threatening complication of diffuse cutaneous systemic sclerosis. Anti-RNA polymerase III strongly correlates with rapidly progressive skin disease and high risk of SRC.
4
Analyze the fourth presentation (proximal weakness, heliotrope rash, ovarian mass).
Identify paraneoplastic dermatomyositis.
Dermatomyositis presenting in an older adult with a solid organ mass strongly suggests a paraneoplastic etiology, which is specifically associated with Anti-TIF1-γ antibodies.

Anahtar Kavram

Targeted autoantibody and specific laboratory test ordering for rheumatologic and systemic autoimmune diseases based on distinct clinical phenotypes.
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