2016
DOI: 10.1016/j.chest.2015.11.004
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Pulmonary Involvement in Patients With Hemophagocytic Lymphohistiocytosis

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Cited by 135 publications
(125 citation statements)
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“…However, after HPS-specific and etiotropic treatments, patients with respiratory function improvement were only 67/118 (56.7%). [23] The results from an autopsy also verified a hemophagocytic phenomenon in the lungs of patients. [25] In this study, the risk of death for patients with pulmonary involvement obviously increased, which was consistent with previous studies.…”
Section: Discussionmentioning
confidence: 88%
See 1 more Smart Citation
“…However, after HPS-specific and etiotropic treatments, patients with respiratory function improvement were only 67/118 (56.7%). [23] The results from an autopsy also verified a hemophagocytic phenomenon in the lungs of patients. [25] In this study, the risk of death for patients with pulmonary involvement obviously increased, which was consistent with previous studies.…”
Section: Discussionmentioning
confidence: 88%
“…A study on children with HPS revealed pleural effusion in 60% patients by imaging. [22] Seguin et al [23] conducted pulmonary high-resolution computed tomography examinations on 68 patients who were diagnosed with HPS, and 38 of them (56%) had pleural effusion. Matthias et al conducted abdominal ultrasound examinations on 9 children who were diagnosed with HPS and observed peritoneal effusion in 6 patients and pleural effusion in 2 patients, [24] indicating that the incidence of serous effusion was high in HPS.…”
Section: Discussionmentioning
confidence: 99%
“…Epidemiologic studies in Japan report the incidence rate at 1 per 800,000 in adults with a median age of 50 years and a male predominance . Published studies note a median survival time of 1.8–2.2 months, and an overall mortality of 42.2% .…”
Section: Discussionmentioning
confidence: 99%
“…Epidemiologic studies in Japan report the incidence rate at 1 per 800,000 in adults with a median age of 50 years and a male predominance [1,2]. Published studies note a median survival time of 1.8-2.2 months, and an overall mortality of 42.2% [3]. Presentation can be diverse, and the primary etiology is unable to be identified in as many as 18% of cases [4].…”
Section: Discussionmentioning
confidence: 99%
“…Progression to ARDS causes Cytokines Release Syndrome (CRS), that is, the upregulation of pro-inflammatory cytokines and chemokines, and this pattern, is very similar to that of secondary haemophagocytic lymphohistiocytosis (sHLH). Approximately around 50% patients' sHLH causes unrelenting fever, cytopenias and hyperferritinaemia, and pulmonary involvement [42,43]. In the majority of severe COVID-19 infections, a sHLH-like cytokine profile has been reported.…”
Section: Pathophysiology and Related Factsmentioning
confidence: 99%