Key result
Two patients with intravascular lymphomatosis presenting as interstitial lung disease showed poor response to chemotherapy and died within 3 months of diagnosis.
Case Report (n=2)
Intravascular lymphomatosis should be included in the differential diagnosis of interstitial lung disease, despite its rarity and poor prognosis.
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Pulmonary intravascular lymphomatosis warrants inclusion in unexplained lung disease differentials; leaves open optimal diagnostic and therapeutic approaches for this rare entity.
Ko et al. (1997) conducted a case report in Intravascular lymphomatosis presenting as interstitial lung disease (n=2). Intravascular lymphomatosis was evaluated on Clinical presentation and mortality. Two patients with intravascular lymphomatosis presenting as interstitial lung disease showed poor response to chemotherapy and died within 3 months of diagnosis.
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