Figure 1. A, The lungs appear unremarkable on day 3 of illness. B, An infiltrate in the right upper lobe was present on day 6 of illness. C, Complete "whiteout" of the right lung field with incipient infiltration on the left along the oblique fissure was present on day 7.
Figure 2. At autopsy the right lung shows complete consolidation with focal involvement along the left oblique fissure, exactly mirroring the chest x-ray film.
Figure 3. A bronchiole (left upper corner) contains desquamated respiratory epithelium and exudate. There is no surrounding lymphocytic infiltrate. The interstitium is congested while the alveoli are filled with macrophages, proteinaceous debris, and necrotic cells (hematoxylin-eosin, original magnification ×40).
Figure 4. Immunohistochemical staining for pertactin demonstrates the organisms localized to the ciliated border on the surface of the bronchiole mucosal epithelium. No organisms were detected in the alveoli (alkaline phosphatase fast red with Harris hematoxylin counterstain, original magnification ×40).
A polymerase chain reaction amplification assay1 confirmed Bordetella pertussis in both premortem and postmortem specimens. Detection of B pertussis using standard microbiologic culture or direct fluorescent antibody detection may be unreliable. Polymerase chain reaction–based assays, while not widely available, have demonstrated increased sensitivity relative to traditional methods2 and have the advantage of remaining positive even after therapy has started.3 In addition, immunohistochemical staining with a monoclonal antibody for pertactin antigen4 demonstrated that the organisms attached to the cilia were B pertussis (Figure 4). Special stains did not show other organisms; no viral inclusions were noted. These findings suggest that B pertussis was the sole infecting agent.
A remarkable feature of this case is the rapid progression of B pertussis pneumonia. Premortem clues to the diagnosis include the absolute lymphocytosis noted on day 3 of illness and the paroxysms of cough interspersed with periods of apparent well-being. In retrospect, earlier administration of erythromycin might have altered the outcome. Suspicion of pertussis on clinical grounds should dictate initiation of treatment until diagnostic testing for the organism is completed.
Pertussis mortality, typically due to pneumonia, is associated with median maternal age of 20 years, gestational age of 36 weeks or less, and age younger than 1 year.5,6 There may be an increased incidence of mortality in Hispanics, presumably as a result of difficulties with communication or genetic or socioeconomic factors. While the mechanism of death is uncertain, perfusion through the consolidated lung may lead to pulmonary hypertension with subsequent right-sided heart failure ending in cardiac arrhythmia.7
Accepted for publication May 1, 1997.
Corresponding author: Mark A. Lovell, MD, Box 168, University of Virginia Health Sciences Center, Charlottesville, VA 22908 (e-mail: firstname.lastname@example.org).
Pathological Case of the Month. Arch Pediatr Adolesc Med. 1998;152(9):926. doi: