Simple Pulmonary Eosinophilia
NORD is very grateful to Evans Fernandez Perez, MD, MS, Autoimmune and Interstitial Lung Disease Center, Division of Pulmonary and Critical Care Medicine, National Jewish Health, for assistance in the preparation of this report.
Synonyms of Simple Pulmonary Eosinophilia
- Loeffler syndrome
- Löffler syndrome
- No subdivisions found.
Simple pulmonary eosinophilia (SPE), also known as Loeffler syndrome, is a rare, temporary (transient) respiratory disorder characterized by the accumulation of eosinophils in the lungs (pulmonary eosinophilia). Eosinophils are a type of white blood cell and are part of the immune system. They are usually produced in response to allergens, inflammation or infection and are particularly active in the respiratory tract. Most cases of SPE are believed to be due to an allergic reaction to drugs and infection (especially parasitic ones). SPE usually ranges in severity from individuals who do not develop any symptoms (outside of eosinophilia) to individuals who develop mild symptoms. In extremely rare cases, more significant complications can occur. Generally, no specific therapy is required as symptoms usually go away spontaneously without treatment.
Simple pulmonary eosinophilia was first described in the medical literature in 1932. It is classified as a form of eosinophilic lung disease, a large group of interstitial lung diseases. SPE is considered a benign, self-limiting disorder.
SPE usually presents as a mild lung disorder characterized by a dry, unproductive cough and a slight fever. Some affected individuals may cough up a mixture of saliva and mucus (sputum). Symptoms usually resolve on their own without treatment (spontaneous resolution) usually within two weeks to a month. In rare cases, symptoms can persist for months especially in the setting of antigen re-exposure.
Additional symptoms can occur in some cases including chest pain, wheezing, shortness of breath (dyspnea), and a rapid breathing rate. Some individuals may complain of a general feeling of poor health (malaise). Inflammation of the mucous membranes of the nose (rhinitis), unintended weight loss and night sweats have also been reported.
According to the medical literature, some individuals with SPE develop acute eosinophilic pneumonia (AEP). AEP is a rare, serious lung disorder that can quickly progress to cause acute respiratory failure. (For more information on AEP, see the related disorders section below).
Generally, SPE is caused by an allergic reaction. A variety of factors including parasitic infection, exposure to certain drugs or exposure to certain fungi have been linked to SPE. In some cases of SPE, the triggering event or cause of SPE is unknown (idiopathic). The exact reason why there is an overproduction and accumulation of eosinophils in the lungs in individuals with SPE is not fully understood.
Most cases are caused by the passage of parasitic larva through the lungs, which result in an allergic reaction. Parasitic worms (helminths) such as nematodes are the most common parasitic cause associated with SPE. The term nematode is a classification (i.e., phylum) of worms characterized by long, round, generally smooth bodies. Nematodes that have been linked to SPE include hookworms and Ascaris lumbricoides, a type of roundworm.
Drugs that have been linked to cases of SPE include nonsteroidal anti-inflammatory drugs (NSAIDs), certain antibiotics, anti-microbials, and anti-seizure medications (anticonvulsants).
Some cases of SPE have been caused by exposure to certain fungi such as Aspergillus fumigatus.
SPE affects males and females in equal numbers. The exact incidence and prevalence of SPE in the general population is unknown. It is the most common form of eosinophilic lung disease. SPE can affect individuals of any age.
Symptoms of the following disorders can be similar to those of SPE. Comparisons may be useful for a differential diagnosis.
Eosinophilic lung diseases are a broad group of disorders. These diseases can be broken down into types without a known cause (idiopathic) and those with a known cause. Eosinophilic lung diseases without a known cause include AEP, chronic eosinophilic pneumonia (CEP), and idiopathic hypereosinophilic syndrome. Known causes of eosinophilic lung disease include allergic bronchopulmonary aspergillosis, exposure to parasitic infections, drugs, or toxic substances and systemic disorders such as Churg-Strauss syndrome and hypereosinophilic syndorme. (For more information on these disorders, choose the specific disorder name as your search term in the Rare Disease Database.)
A diagnosis of SPE is based upon identification of characteristic symptoms (e.g., eosinophilic pneumonia), a detailed patient history, a thorough clinical evaluation, the absence of other known causes of eosinophilic lung disease, and a variety of specialized tests. A physical examination may reveal wheezing and/or a rattling sound in the lungs (rales). Distinguishing SPE from other, more severe forms of pulmonary eosinophilia is especially important when obtaining a diagnosis.
Clinical Testing and Work-Up
Imaging techniques may be used to help confirm a diagnosis of SPE including chest x-ray or computerized tomography (CT) scanning. Chest x-rays in individuals with SPE generally show white patches or shadows (infiltrates) in the lungs. These infiltrates may disappear, but can reappear in different areas of the lungs. A CT scan may reveal hazy areas (ground-glass opacities) that are not seen on traditional x-rays. During CT scanning, a computer and x-rays are used to create a film showing cross-sectional images of certain tissue structures such as the lungs. A CT scan can also show airspace consolidation, in which the tiny air sacs of the lungs (alveolar) become abnormally filled (as with eosinophils).
A procedure known as bronchoalveolar lavage (BAL) may also be used to help obtain a diagnosis of SPE. During BAL, a narrow tube (bronchoscope) is slid down the windpipe into the lungs and a sterile solution is passed through the tube washing out (lavaging) cells. This fluid is collected and then the tube is removed, allowing the cells to be studied. BAL in individuals with SPE reveals abnormally high levels of eosinophils.
Blood tests may reveal mildly elevated levels of eosinophils and/or serum immunoglobulin E (IgE). A stool examination may reveal the presence of parasites. Analysis of sputum or fluid obtained from pumping the stomach (gastric lavage) may reveal parasitic larvae.
Additional tests may be performed to rule out other causes of pulmonary eosinophilia.
In most cases, no treatment is required and SPE goes away on its own (spontaneous remission). Cases due to active parasitic infection should be treated with appropriate anti-parasitic medications. Drug-induced cases should be treated by stopping the offending medication. In rare cases, corticosteroid therapy may be required and is generally highly effective. In some cases, SPE will recur.
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.
For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Tollfree: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
Simple Pulmonary Eosinophilia Resources
Please note that some of these organizations may provide information concerning certain conditions potentially associated with this disorder.
NORD Member Organizations:
(To become a member of NORD, an organization must meet established criteria and be approved by the NORD Board of Directors. If you're interested in becoming a member, please contact Susan Olivo, Membership Manager, at email@example.com.)
Cordier JF, Cottin V. Eosinophilic Pneumonias. In: Interstitial Lung Disease, 5th ed. Schwarz MI, King Jr. TE, eds. 2011, People's Medical Publishing House, Shelton, CT. pp. 833-893
Cottin V. Idiopathic eosinophilic pneumonias. In: European Respiratory Monograph: Clinical Handbooks for the Respiratory Professional. Orphan Lung Diseases. Cordier JF, ed. 2011, European Respiratory Society, United Kingdom. pp. 118-139.
Leitch AG. Pulmonary Eosinophilias. In: Crofton and Douglas's Respiratory Diseases 2, 5th ed. Seaton A, Seaton D, Leitch AG, eds. 2000, Blackwell Science, Malden, MA. pp. 1020-1034.
Fernández Pérez ER, Olson AL, Frankel SK. Eosinophilic lung diseases. Med Clin North Am. 2011;95:1163-87.
Campos LE, Pereira LF. Pulmonary eosinophilia. J Bras Pneumol. 2009;35:561-573. http://www.ncbi.nlm.nih.gov/pubmed/19618037
Jeong YJ, Kim KL, Seo IJ, et al. Eosinophilic lung diseases: a clinical, radiologic, and pathologic overview. Radiographics. 2007;27:617-637. http://www.ncbi.nlm.nih.gov/pubmed/17495282
Alberts WM. Eosinophilic interstitial lung disease. Curr Opin Pulm Med. 2004;10:419-424. http://www.ncbi.nlm.nih.gov/pubmed/15316442
Fujimura J, Murakami Y, Tsuda A, et al. A neonate with Löffler syndrome. J Perinatol. 2001;21:207-208. http://www.nature.com/jp/journal/v21/n3/abs/7200507a.html
Sharma GD, Vinikoor MJ. Loffler syndrome. Emedicine Journal, February 1, 2010. Available at: http://emedicine.medscape.com/article/1002606-overview Accessed January 5, 2012.
Newman LS. Eosinophilic Pneumonia. The Merck Manual Home Health Handbook. September 2006. Available at: http://www.merckmanuals.com/home/index.html Accessed January 5, 2012.
The information in NORD’s Rare Disease Database is for educational purposes only. It should never be used for diagnostic or treatment purposes. If you have questions regarding a medical condition, always seek the advice of your physician or other qualified health professional. NORD’s reports provide a brief overview of rare diseases. For more specific information, we encourage you to contact your personal physician or the agencies listed as “Resources” on this report.
The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.
Copyright ©1989, 2000, 2012
Report last updated: 2012/04/24 00:00:00 GMT+0
NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.