Abstract

The combination of schistosomiasis and pulmonary hypertension (PH) was always recognized as a very rare one; in medical literature, PH is considered as a manifestation of hepatosplenic schistosomiasis but not a manifestation of schistosomal infection until recently. Only 18.5% of patients that have a documented hepatosplenic schistosomiasis were found with PH. Schistosomiasis rarely causes PH without evident hepatosplenic manifestations. Here, we are reporting a case of a patient whose first clinical presentation was features of PH. We use this case as an opportunity to outline pathological mechanisms, causes and classification of PH. A structured and thorough workup for PH is emphasized. It is important to exclude all other secondary causes to be able to diagnose primary PH especially in the absence of a positive family history and advanced diagnostic technology.

Highlights

  • Pulmonary hypertension (PH) is considered when the mean pulmonary artery pressure at rest is equal or more than 25 mm Hg [1]

  • The combination of schistosomiasis and pulmonary hypertension (PH) was always recognized as a very rare one; in medical literature, PH is considered as a manifestation of hepatosplenic schistosomiasis but not a manifestation of schistosomal infection until recently

  • We describe the rare case of a patient who was presented with PH secondary to schistosomal infection without any identifiable symptoms or signs of hepatosplenic disease

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Summary

Introduction

Pulmonary hypertension (PH) is considered when the mean pulmonary artery pressure at rest is equal or more than 25 mm Hg [1]. The combination of schistosomiasis and pulmonary hypertension (PH) was always recognized as a very rare one; in medical literature, PH is considered as a manifestation of hepatosplenic schistosomiasis but not a manifestation of schistosomal infection until recently. Schistosomiasis rarely causes PH without evident hepatosplenic manifestations.

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