Objective: Recent reports have described severe precocious pulmonary emphysema in persons who inject methylphenidate (crushed Ritalin tablets) i.v. We retrospectively evaluated the plain radiographic and CT features in 21 such patients.
Materials And Methods: The chest radiographs, available CT scans, and clinical and pathologic data were reviewed in 21 cases of i.v. Ritalin use. The patients were from 35 to 54 years old. Twelve patients were men, and nine were women. Emphysema was graded on the basis of findings on chest radiographs, by consensus, on a four-point scale as absent, mild, moderate, or severe. CT scans were available for three patients, including one imaged after a single lung transplantation. Autopsy results were available for four patients. Fixed inflated lung specimens and corresponding high-resolution CT scans were available in three cases.
Results: Radiographs showed pulmonary emphysema in all cases. The distribution of disease was basilar and symmetric. Small apical bullae were suggested in only one case. Basilar emphysema was rated as mild in four patients, moderate in three patients, and severe in 14 patients. In 11 patients who had serial chest radiographs, the basilar emphysema was noted to progress over a 2- to 7-year period. No evidence of progressive massive fibrosis was seen in any patient. CT scans confirmed emphysema, most severe at the lung bases.
Conclusion: The plain radiographic and CT findings in patients who inject Ritalin are similar to those found in patients with alpha 1-antitrypsin deficiency and different from the findings seen in other types of i.v. drug use. The finding of basilar pulmonary emphysema should alert the radiologist to the possibility of i.v. injection of Ritalin.
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http://dx.doi.org/10.2214/ajr.162.3.8109495 | DOI Listing |
Chest
January 2025
Division of Respirology, Critical Care and Sleep Medicine, Department of Medicine, University of Saskatchewan, Saskatoon, SK, Canada.
Alpha-1-Antitrypsin (A1AT) deficiency is a common hereditary disorder associated with increased risk of developing chronic obstructive pulmonary disease (COPD). Many individuals with severe A1AT deficiency go undiagnosed, or are diagnosed late, and fail to benefit from disease-specific counseling and modifying care. Since the 2012 Canadian Thoracic Society (CTS) A1AT deficiency clinical practice guideline, new approaches to optimal diagnosis using modern genetic testing and studies of A1AT augmentation therapy have been published.
View Article and Find Full Text PDFAm J Respir Crit Care Med
January 2025
University of Minnesota, Medicine, Minneapolis, Minnesota, United States.
Cureus
December 2024
Internal Medicine, Mercy Health St. Vincent Medical Center, Toledo, USA.
We present a case of spontaneous hemorrhage in an emphysematous bulla, complicated by anticoagulation. Bullous emphysema is a well-recognized complication of chronic obstructive pulmonary disease (COPD), and a rare manifestation is hemorrhage into preexisting pulmonary bullae. A 69-year-old male patient presented to the emergency department with hemoptysis, shortness of breath, and productive cough.
View Article and Find Full Text PDFBMC Pulm Med
January 2025
State Key Laboratory of Respiratory Disease & National Clinical Research Center for Respiratory Disease & National Center for Respiratory Medicine & Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510120, China.
Background: Studies on consistency among spirometry, impulse oscillometry (IOS), and histology for detecting small airway dysfunction (SAD) remain scarce. Considering invasiveness of lung histopathology, we aimed to compare spirometry and IOS with chest computed tomography (CT) for SAD detection, and evaluate clinical characteristics of subjects with SAD assessed by these three techniques.
Methods: We collected baseline data from the Early COPD (ECOPD) study.
Background: Pulmonary Langerhans Cell Histiocytosis (PLCH) is a rare interstitial lung disease primarily affecting young to middle-aged smokers. While traditionally linked to tobacco use, there is growing evidence that cannabis use may contribute to PLCH.
Methods: We present a case of a 52-year-old male with PLCH associated with heavy cannabis use.
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