Pneumocystis jirovecii pneumonia in an HIV-infected patient mimicking acute eosinophilic pneumonia: a case report with a review of the literature
Case Report

Pneumocystis jirovecii pneumonia in an HIV-infected patient mimicking acute eosinophilic pneumonia: a case report with a review of the literature

Hiroshi Ohji1, Tsutomu Shinohara2, Naoki Kadota1, Yoshio Okano1, Keishi Naruse3, Yoshihito Iwahara4, Fumitaka Ogushi1

1Division of Pulmonary Medicine, 2Department of Clinical Investigation, 3Division of Pathology, 4Division of Hematology, National Hospital Organization Kochi Hospital, Kochi, Japan

Correspondence to: Tsutomu Shinohara. Department of Clinical Investigation, National Hospital Organization Kochi Hospital, 1-2-25 Asakuranishimachi, Kochi 780-8077, Japan. Email: shinohara.tsutomu.kg@mail.hosp.go.jp.

Submitted May 29, 2018. Accepted for publication Sep 29, 2018.

doi: 10.21037/jtd.2018.10.49


Introduction

Pneumocystis jirovecii pneumonia (PCP) is the most common opportunistic infection with the highest lethality among acquired immunodeficiency syndrome (AIDS)-related diseases, and there are many cases where HIV infection is revealed by PCP as an initial manifestation. In Japan, AIDS patients unaware of their HIV status account for approximately 30% of newly diagnosed HIV-positive patients, and the percentage of PCP is the highest at approximately 30% among AIDS-indicator diseases (1,2). Pneumocystis jirovecii interacts with many kinds of host cells in the lung and induces lung injury. Although onset of HIV-positive PCP is usually slow, the clinical presentation including respiratory failure occasionally takes an acute course. The typical chest radiographic finding of PCP is ground-glass opacity (GGO), sometimes accompanied by nodular shadows and/or consolidations (3,4). Therefore, differential diagnosis from various diffuse lung diseases, including progressive interstitial pneumonia, is not always easy. In addition, eosinophilia (greater than or equal to 5 percent) in bronchoalveolar lavage (BAL) fluid (BALF) has been observed in about 20% of HIV-positive PCP patients (5).

Acute eosinophilic pneumonia (AEP) is a disease concept proposed by Allen et al. in 1989 and characterized by fever, diffuse pulmonary infiltrates (GGO with or without air-space consolidation) and BALF eosinophilia (greater than 25 percent) in an acute course, leading to a high rate of respiratory failure (6,7). Although AEP is idiopathic, it is favorable for young adult males and a relationship with smoking has been reported in a number of cases. Thus, AEP is presumed to be an acute hypersensitivity reaction to some inhaled antigen and, in general, steroid therapy is effective (6).

In this manuscript, we report a HIV-positive PCP case with prominent BALF eosinophilia (38.5%), which was initially treated as AEP, and discuss the usefulness of serum and BALF biomarkers for pneumonitis, such as serum surfactant protein D (SP-D) and Krebs von den Lungen-6 (KL-6), in the diagnosis of this condition.


Case presentation

A 44-year-old man in previous good health was admitted to our hospital due to a 1-week history of dyspnea and fever without severe fatigue, muscle weakness or weight loss. The patient had no clinical history of sexually transmitted disease or fungal infection, and had not received any medication. He smoked ten cigarettes a day for 1 year about 20 years earlier. Physical examination revealed slightly decreased breath sounds in both lungs. Laboratory data were as follows: white blood cell count, 6,880/µL [neutrophils, 59.7%; lymphocytes, 32.4% (2.2×103/L); eosinophils, 2.6%; monocytes, 0.0%; basophils, 0.4%]; hemoglobin, 15.1 g/dL; platelet count, 14.0×104/µL; C-reactive protein, 0.98 mg/dL; SP-D, 90.1 [<107 (8)] ng/mL; serum KL-6, 2,330 [<476 (8)] U/mL. Mild hypoxemia (SpO2 94% on room air) was noted, but there were no other signs of HIV or opportunistic infection, such as LDH elevation and liver disorder. Chest X-ray and high-resolution CT showed bilateral GGOs without chronic changes (Figure 1). Bronchoscopic examination was performed on suspicion of interstitial pneumonia and BAL (recovery rate; 64/150) revealed high total cellularity (42×104 cells/mL) consisting of 38.5% eosinophils, 37.5% neutrophils, 16.5% lymphocytes and 7.5% alveolar macrophages. BALF smear and culture showed normal flora and transbronchial lung biopsy (TBLB) detected no specific findings. AEP was clinically suspected and the patient was treated with oral prednisolone (30 mg/day). However, his respiratory condition worsened (SpO2 92% at rest receiving oxygen via a non-rebreather mask at 12 L/min) and GGOs clearly progressed over two weeks (Figure 1). Methylprednisolone pulse therapy (1,000 mg intravenously for 3 days) was added. Then, a highly elevated (1→3)-β-D-glucan (BDG) level [185 pg/mL: cut-off level was 20 pg/mL (9)] in the serum was observed. Additional sectioning of the TBLB specimen revealed eosinophilic foamy areas on hematoxylin and eosin staining and accumulation of black-colored cysts on Grocott methenamine silver stain in alveolar lesion (Figure 2A,B). No findings suggesting cytomegalovirus pneumonia, such as nuclear inclusion bodies, were observed in the lung tissue. Polymerase chain reaction (PCR) analysis of sputum was positive for Pneumocystis jirovecii. The serum anti-HIV-1 antibody was positive and peripheral blood CD4-positive lymphocytes decreased to 18/L. HIV-1 western blot analysis was positive and real-time PCR assay revealed a HIV-1 RNA of 7.3×104 copy/mL. Cytomegalovirus (CMV) antigenemia was positive. Additional examination of BALF showed that the concentrations of BDG, SP-D and KL-6 were 1,010 pg/mL, 804 ng/mL and 5,626 U/mL respectively [cut-off levels of BALF BDG and SP-D were not described previously (10,11), but that of KL-6 was 340 (12)]. PCP and CMV infection complicated with AIDS was diagnosed. Trimethoprim-sulfamethoxazole, atovaquone and ganciclovir were administered followed by anti-HIV therapy (raltegravir and emtricitabine/tenofovir disoproxil fumarate). Hypoxemia and abnormal findings on chest X-ray improved after 3 months of this treatment (Figure 1).

Figure 1 Chest X-ray (A, D and E) and high-resolution CT (B and C) findings. (A,B,C) Bilateral ground-glass opacities (GGOs) without chronic changes on admission to hospital; (D) worsening of pre-existing GGOs two weeks after the initiation of treatment using oral prednisolone (30 mg/day); (E) marked improvement after 3 months of treatment (administration of trimethoprim-sulfamethoxazole, atovaquone and ganciclovir followed by anti-HIV therapy).
Figure 2 Pathological findings of transbronchial lung biopsy specimens (A, hematoxylin and eosin staining; B, Grocott methenamine silver staining). (A) Eosinophilic foamy areas in alveolar lesions; (B) accumulation of black-colored cysts.

Discussion

HIV-positive PCP occasionally resembles AEP in terms of clinical symptoms, chest radiographic findings and BALF cell classification. Both diseases may progress rapidly and cause severe respiratory failure, but the treatments for each disease are fundamentally different and prompt differentiation is important.

There are many PCP patients who do not know that they are infected with HIV and these patients do not always have accompanying peripheral blood lymphopenia. It was reported that peripheral blood absolute lymphocyte count (ALC) was 1.1×103/µL or more in 25% of cases where HIV infection was revealed by PCP and, as observed in our patient, ALC in 7.5% of the cases was more than 2.0×103/L (13). Generally, distribution of GGO shows central predominance in HIV-positive PCP, whereas in AEP it shows peripheral predominance. However, in half the patients with each disease, the distribution does not meet this trend, and consolidations, interlobular septal thickening and nodules are common findings in both diseases (3,7). These reports suggest that further insight into differentiation between HIV-positive PCP and AEP is necessary.

BDG is a major constituent of the cell wall in pneumocystis jirovecii, and it was reported that both serum and BALF BDG levels are elevated in HIV-positive PCP (Table 1), as shown in our case (10,15,16). However, even in HIV-positive PCP cases, no increase in concentration of serum BDG was observed in about 5% of cases (10,15,16). On the other hand, Kawayama et al. reported that BDG did not increase in serum in AEP, but rose in BALF (Table 1). The authors considered the possibility that BDG inhaled from the environment directly acted as a biological response modifier and induced eosinophilic inflammation in the alveolus (11). Thus, it is not always easy to distinguish between HIV-positive PCP and AEP with only BALF and serum BDG values.

Table 1
Table 1 BDG, SP-D and KL-6 levels in the serum/BALF of an HIV-positive PCP and AEP case
Full table

In cases where serum BDG has not yet been measured or is in the normal range and in whom bronchoscopic examination has not been performed, one differential diagnosis of HIV-positive PCP or AEP is progressive interstitial pneumonia and, in routine practice, evaluation of markers for pneumonitis such as SP-D and KL-6 is usually done. SP-D is a glycoprotein mainly produced in type II alveolar epithelial cells and is directly secreted into the alveolar spaces. On pulmonary injury, the efflux of SP-D from damaged epithelial secretory cells into the alveoli and its sift into the blood due to the increased permeability of lung vessels induce the elevated serum SP-D level (19). On the other hand, KL-6 is a cell membrane constituent glycoprotein with a huge molecular weight, and mainly expressed in type II alveolar epithelial cells and bronchiolar epithelium. When alveolar epithelium is strongly injured due to fibrosing interstitial pneumonia etc., the production of KL-6 by regenerating type II alveolar epithelial cells is enhanced, and KL-6 cleaved just outside the cell membrane accumulate in the alveolar space. Then KL-6 transfers to the blood like SP-D (20).

Daimon et al. reported that serum and BALF SP-D levels were elevated in AEP, but KL-6 levels were within normal range (Table 1) (14). These data probably reflect the fact that there is no strong alveolar epithelial injury in AEP. In contrast, a clinical study revealed that the concentration of serum KL-6 was high in HIV-positive PCP, probably reflecting epithelial injury, although BALF KL-6 was not measured (Table 1) (15). In this case, KL-6 was elevated in both BALF and serum, suggesting that KL-6 is a marker for HIV-positive PCP even in cases showing prominent BALF eosinophilia. An elevated level of SP-D was observed only in BALF but not in serum, the reasons for which are unclear at this time. However, up-regulation of BALF SP-D may reflect a host defense mechanism enhancing opsonization in interactions between Pneumocystis jirovecii and alveolar macrophages rather than an extensive type II epithelial cells injury (21). To the best of our knowledge, there are three reported cases of HIV-positive PCP mimicking AEP, two of which indicated an elevated serum level of KL-6. However, the significance was not discussed (Table 1) (17,18). The accumulation of similar cases is necessary to evaluate the specificity and sensitivity of KL-6 as a biomarker of HIV-positive PCP with prominent BALF eosinophilia.


Conclusions

For patients who present with an acute course with GGO, prominent BALF eosinophilia, and elevated BALF and/or serum KL-6 level(s), we need to consider HIV-positive PCP, even when peripheral blood lymphopenia is not observed.


Acknowledgements

We would like to thank Mikio Miyauchi (Division of Clinical Laboratory, National Hospital Organization Kochi Hospital) for his contribution.


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.

Informed Consent: Written informed consent was obtained from the patient for publication of this manuscript and any accompanying images.


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Cite this article as: Ohji H, Shinohara T, Kadota N, Okano Y, Naruse K, Iwahara Y, Ogushi F. Pneumocystis jirovecii pneumonia in an HIV-infected patient mimicking acute eosinophilic pneumonia: a case report with a review of the literature. J Thorac Dis 2018;10(11):E774-E778. doi: 10.21037/jtd.2018.10.49