eMedicine Specialties > Oncology > Special Topics in Oncology

Pel-Ebstein Fever

Ephraim P Hochberg, MD, Instructor in Medicine, Cancer Center, Massachusetts General Hospital

Updated: Jun 26, 2006

Introduction

Background

Hodgkin lymphoma (HL) is an unusual lymphoma that can manifest with constitutional symptoms (eg, fever, weight loss, night sweats) termed B-type symptoms. The periodic fever associated with HL is known as the Pel-Ebstein fever.

The criteria for B-type symptoms include fever (ie, temperature >38°C [>100.4°F]) for 3 consecutive days, weight loss exceeding 10% of body weight in 6 months, and night sweats. Pruritus, previously considered an important systemic symptom, does not by itself have prognostic importance and is not sufficient on its own to classify a patient as possessing B-type symptoms.

Pathophysiology

The pathophysiologic mechanism of the Pel-Ebstein fever is unknown; however, it is presumed to be due to cyclic cytokine release.

Frequency

United States

No reliable objective data are known regarding the occurrence rate of classic Pel-Ebstein fever in a series of patients with HL. Anecdotally, some authorities estimate a 5-10% occurrence rate.

International

US and international rates of Pel-Ebstein fever are not known to differ.

Mortality/Morbidity

  • The Pel-Ebstein fever is not an independent cause of either morbidity or mortality, although the high fevers can be quite uncomfortable.
  • The episodic hemolysis sometimes associated with Pel-Ebstein fever has been suggested to be due to increased susceptibility of older erythrocytes to temperature-induced hemolysis. Two cases of Pel-Ebstein fever temporally associated with pancytopenia have been reported, which would seem to suggest a cytokine-mediated etiology.

Race

No evidence indicates that Pel-Ebstein fever manifests differently or with different frequencies according to race.

Sex

Pel-Ebstein fever is not known to be sex-linked.

Age

No frequency differences by age group are known.

Clinical

History

  • Pel-Ebstein fever was described by 2 physicians in the late 1800s.
    • Wilhelm Ebstein, a German internist who was a professor of medicine in Göttingen, described a patient with relapsing fever in "Das chronische Rückfallsfieber, eine neue Infektionskrankheit." Berliner klinische Wochenschrift, 1887, 24: 565-8, 837.
    • Pieter Pel was a physician in Amsterdam who noted a similar finding years earlier in "Zur Symptomatologie der sogenannten Pseudo-Leukãmie." Berliner klinische Wochenschrift, 1885, 22: 3-7.
  • Pel-Ebstein fever has been used as an example of a disease that exists only because it has a name.

Physical

  • The diagnosis of Pel-Ebstein fever is made by examining a patient's temperature over several weeks.
  • The classic description is of a relapsing, high-grade fever that can reach 40-40.5°C (105-106°F) and has a periodicity of 7-10 days. The fever spikes are abrupt in onset and resolution. The fever spikes overlie a temperature baseline that never quite reaches normal.
  • Multiple, evenly spaced Beau lines in the nailbeds have been described as indicative of relapsing fever.

Causes

  • The etiology of Pel-Ebstein fever is thought to be cytokine release. Cytokines known to be released by Reed-Sternberg cells include interleukin 13, macrophage colony-stimulating factor, transforming growth factor-alpha, interleukin 10, and the T cell–directed CC chemokine thymus- and activation-regulated chemokine. Monocyte chemotactic protein 1 and interleukin 8 have also been detected at increased levels in HL tissues.

Differential Diagnoses

Abdominal Abscess
Dengue Fever
Amebiasis
Echoviruses
Arenaviruses
Enterobacter Infections
Bronchitis
Enterococcal Infections
Carcinoid Lung Tumors
Factitious Disorder
Carcinoid Tumor, Intestinal
Fever of Unknown Origin
Catscratch Disease
Human Herpesvirus Type 6
Cellulitis
Hypersensitivity Reactions, Delayed
Chagas Disease (American Trypanosomiasis)
Hypersensitivity Reactions, Immediate
Chronic Bronchitis
Inflammatory Bowel Disease
Coxsackieviruses
Cryptococcosis

Other Problems to Be Considered

Pancreatic carcinoid tumor

Workup

Laboratory Studies

  • In a patient with true Pel-Ebstein fever, the diagnosis is established by the histologic finding of HL or another lymphoma. (Other lymphomas and malignancies may be associated with fevers, but only the fever associated with HL is named Pel-Ebstein.)
  • No laboratory tests are particularly useful in persons with Pel-Ebstein fever.
  • In rare cases, Pel-Ebstein fever has been associated with episodic hemolysis. In these cases, hemolysis laboratory studies may be helpful in making a diagnosis.

Imaging Studies

  • Imaging studies are not useful in the diagnosis of the fever; however, CT scans of the neck, chest, abdomen, and pelvis, as well as PET or gallium scans, can be useful in the diagnosis of the underlying Hodgkin lymphoma.

Procedures

  • No diagnostic procedures are particularly useful in persons with Pel-Ebstein fever beyond the biopsy used to diagnose the HL or causative lymphoma.

Treatment

Medical Care

  • Therapy for Pel-Ebstein fever involves the following 2 concepts:
    • Standard antipyretic regimens, including aspirin and nonsteroidal anti-inflammatory drugs
    • Most importantly, chemotherapy for the underlying lymphoma
  • Pel-Ebstein fever reportedly responds to chemotherapy within as short as 2 days.

Surgical Care

Surgery is not indicated.

Consultations

Consulting a hematologist or oncologist for the management of the underlying HL is mandatory.

Diet

Diet modification is ineffective in the therapy for Pel-Ebstein fever.

Activity

Activity restriction does not play a role in treatment of Pel-Ebstein fever.

Medication

Antipyretic therapy and chemotherapy for the underlying lymphoma are the 2 mainstays of medical therapy for Pel-Ebstein fever. Treatment of the underlying lymphoma or Hodgkin lymphoma (HL) is beyond the scope of this discussion (see Hodgkin Disease).

Antipyretic agents

These agents are used to reduce uncomfortable fevers.


Acetaminophen (Tylenol)

Reduces fever by acting directly on hypothalamic heat-regulating centers, which increases dissipation of body heat via vasodilation and sweating.

Dosing

Adult

325-1000 mg PO q4h prn; not to exceed 4 g/d

Pediatric

10-15 mg/kg/dose PO q4-6h; not to exceed 5 doses/d

Interactions

Rifampin can reduce analgesic effects; barbiturates, carbamazepine, hydantoins, and isoniazid may increase hepatotoxicity

Contraindications

Documented hypersensitivity

Precautions

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

Hepatotoxicity possible in chronic alcoholism following various dose levels; severe or recurrent pain or high or continued fever may indicate serious illness; acetaminophen is contained in many OTC products, and combined use with these products may result in cumulative doses exceeding recommended maximum dose

Follow-up

Further Inpatient Care

  • No particular inpatient requirements are indicated for the management of Pel-Ebstein fever.

Further Outpatient Care

  • No particular outpatient therapy is warranted.

Inpatient & Outpatient Medications

  • Antipyretics are a mainstay of therapy, along with chemotherapy for HL.

Complications

  • Several reported cases of hemolysis have been associated with Pel-Ebstein fever. Whether the degree of hemolysis is inappropriate for the degree of fever or whether this is merely a temperature-related hemolytic reaction has not been determined. Additionally, 2 cases of cyclic pancytopenia have been reported.

Prognosis

  • B-type symptoms are a negative prognostic factor for HL.

Patient Education

  • Patients should be educated on the appropriate timing of antipyretic therapy.

Miscellaneous

Medicolegal Pitfalls

  • The differential diagnosis of relapsing fever is a possible source of malpractice liability.

References

  1. Colvett KL, Patel D, Smith JK. Multiple Beau''s lines in a patient with fever of unknown origin. South Med J. Dec 1993;86(12):1424-6. [Medline].

  2. Dankbaar H, Willemze R, Bieger R. Bone marrow disorders in Hodgkin''s disease: cyclic pancytopenia coinciding with Pel-Ebstein fever. Neth J Med. 1983;26(3):74-6. [Medline].

  3. Good GR, DiNubile MJ. Images in clinical medicine. Cyclic fever in Hodgkin''s disease (Pel- Ebstein fever). N Engl J Med. Feb 16 1995;332(7):436. [Medline].

  4. Hilson AJ. Pel-Ebstein fever [letter; comment]. N Engl J Med. Jul 6 1995;333(1):66-7. [Medline].

  5. Koopmans RP, van den Born BJ, Kersten MJ, Hart W. [Clinical reasoning and decision making in practice. A 41-year old with periodic fever of unknown origin]. Ned Tijdschr Geneeskd. Sep 13 2003;147(37):1778-83. [Medline].

  6. McKenna W, Lampert I, Oakley C, Goldman J. Pel-Ebstein fever coinciding with cyclical haemolytic anaemia and splenomegaly in a patient with Hodgkin''s disease. Scand J Haematol. Nov 1979;23(5):378-80. [Medline].

  7. Molina Boix M, Ortega Gonzalez G, Garcia Perez B, Perez Gracia A. [Pel-Ebstein fever, hemolytic anemia and Hodgkin''s disease (letter)]. An Med Interna. Jul 1989;6(7):388-9. [Medline].

  8. Racchi O, Rapezzi D, Ferraris AM, Gaetani GF. Unusual bone marrow relapse of Hodgkin''s disease with typical Pel- Ebstein fever. Ann Hematol. Jul 1996;73(1):39-40. [Medline].

  9. Reimann HA. Periodic (Pel-Ebstein) fever of lymphomas. Ann Clin Lab Sci. Jan-Feb 1977;7(1):1-5. [Medline].

  10. Storgaard L, Karle H. Fever and haemolysis in Hodgkin''s diseases. Acta Med Scand. Apr 1975;197(4):311-6. [Medline].

  11. Talbot TR. Cases from the Osler Medical Service at Johns Hopkins University. Hodgkin''s disease with Pel-Ebstein fevers. Am J Med. Mar 2002;112(4):312-3. [Medline].

Keywords

Pel-Ebstein fever, periodic fever of lymphomas, Hodgkin disease, Hodgkin's disease, HD, Hodgkin's episodic fever, Hodgkin episodic fever, B symptoms, B-type symptoms, Hodgkin lymphoma, Hodgkin's lymphoma, HL, lymphoma, lymphoma-related fever, relapsing fever, hemolysis, hemolytic anemia, periodic fever spikes

Contributor Information and Disclosures

Author

Ephraim P Hochberg, MD, Instructor in Medicine, Cancer Center, Massachusetts General Hospital
Ephraim P Hochberg, MD is a member of the following medical societies: American Society of Clinical Oncology and American Society of Hematology
Disclosure: Nothing to disclose.

Medical Editor

Jeffrey M Zaks, MD, Clinical Associate Professor of Medicine, Wayne State University School of Medicine; Vice President, Medical Affairs, Chief Medical Officer, Department of Internal Medicine, Providence Hospital
Jeffrey M Zaks, MD is a member of the following medical societies: American College of Cardiology, American College of Healthcare Executives, American College of Physician Executives, and American Medical Association
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Joseph F John Jr, MD, FACP, FIDSA, FSHEA, Professor of Medicine, Molecular Genetics and Microbiology, Medical University of South Carolina; Associate Chief of Staff for Education, Ralph H Johnson Veteran's Administration Medical Center
Disclosure: BioMerieux Honoraria Review panel membership; Cubist Honoraria Review panel membership; Pfizer Honoraria Speaking and teaching; Merck Stock dividends stock holdings

CME Editor

Eleftherios Mylonakis, MD, Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital
Eleftherios Mylonakis, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Society for Microbiology, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

Chief Editor

John S Macdonald, MD, Professor of Medicine, New York Medical College; Chief, Division of Medical Oncology, St Vincent's Hospital and Medical Center; Medical Director, Saint Vincent's Comprehensive Cancer Center
Disclosure: Nothing to disclose.

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