Cat scratch disease
|Cat scratch disease|
|Classification and external resources|
Cat scratch disease (CSD), also known as cat scratch fever, Teeny's Disease, inoculation lymphoreticulosis, and subacute regional lymphadenitis, is a common and usually benign infectious disease caused by the fastidious intracellular gram negative bacterium Bartonella henselae or Bartonella quintana. It is most commonly found in children following a scratch or bite from a cat within about one to two weeks.
Signs and symptoms
Cat scratch disease commonly presents as tender, swollen lymph nodes near the site of the inoculating bite or scratch and is usually limited to one side. This condition is referred to as regional lymphadenopathy and occurs 1-3 weeks after inoculation. Lymphadenopathy in CSD most commonly occurs in the arms, neck, or jaw, but may also occur near the groin or around the ear. There may be a vesicle or an erythematous papule at the site of initial infection. Most patients also develop systemic symptoms such as malaise, decreased appetite, and aches. Other associated complaints include headache, chills, muscular pains, joint pains, arthritis, backache and abdominal pain. It may take 7 to 14 days, or as long as two months, before symptoms appear. Most cases are benign and self-limiting, but lymphadenopathy may persist for several months after other symptoms disappear. The disease usually resolves spontaneously, with or without treatment, in one month.
In rare situations, Cat scratch disease can lead to the development of serious neurologic or cardiac sequelae such as meningoencephalitis, encephalopathy, seizures, or endocarditis. Endocarditis associated with bartonella infection has a particularly high mortality. Parinaud's oculoglandular syndrome is the most common ocular manifestation of Cat scratch disease and is a granulomatous conjunctivitis with concurrent swelling of the lymph node near the ear. Optic neuritis may also occur.
Immunocompromised patients are susceptible to other conditions associated with Bartonella henselae and Bartonella quintana such as [Bacillary angiomatosis]] or Bacillary peliosis. Bacillary angiomatosis is primarily a vascular skin lesion that may extend to bone or be present in other areas of the body. In the typical scenario, the patient has HIV or another cause of severe immune dysfunction. Bacillary peliosis is a condition caused by B. Henselae that most-often affects patients with HIV and other conditions causing severe immune compromise. The liver and spleen are primarily affected, with findings of blood-filled cystic spaces on pathology.
The Warthin–Starry stain can be helpful to show the presence of B. henselae, but is often difficult to interpret. B. Henselae is difficult to culture and can take 2-6 weeks to incubate. The best diagnostic method currently available is Polymerase chain reaction (PCR), which has a sensitivity of 43-76% and a specificity (in one study) of 100%.
Kittens are more likely to carry the bacteria in their blood, and may therefore be more likely to transmit the disease than adult cats. However, the results of experimental studies showed that fleas serve as a vector for transmission of B. henselae among cats, and that viable B. henselae are excreted in the feces of Ctenocephalides felis, the cat flea. Another study showed that cats could be infected with B. henselae through intradermal inoculation using flea feces containing B. henselae. As a consequence, it is believed that a likely means of transmission of B. henselae from cats to humans may be inoculation with flea feces containing B. henselae through a contaminated cat scratch wound or by cat saliva transmitted in a bite. Ticks can also act as vectors and occasionally transmit the bacteria to humans.
Cat scratch disease is characterized by granulomatous inflammation on histological examination of the lymph nodes. Under the microscope, the skin lesion demonstrates a circumscribed focus of necrosis, surround by histiocytes, often accompanied by multinucleated giant cells, lymphocytes, and eosinophils. The regional lymph nodes demonstrate follicular hyperplasia with central stellate necrosis with neutrophils, surrounded by palisading histiocytes (suppurative granulomas) and sinuses packed with monocytoid B cells, usually without perifollicular and intrafollicular epithelioid cells. This pattern although typical is only present in a minority of cases.
Most healthy people will clear the infection without treatment, and antimicrobial therapy is not recommended for immunocompetent patients with mild to moderate Bartonella henselae disease due to the risk of side-effects from antibiotics. Azithromycin, ciprofloxacin, doxycycline, gentamicin, rifampicin, and trimethoprim/sulfamethoxazole have been used, but have demonstrated limited efficacy.
Azithromycin is preferentially used in pregnancy to avoid the teratogenic side-effects of doxycycline. However, doxycycline is preferred to treat B. henselae infections with optic neuritis due to doxycycline's ability to adequately penetrate the tissues of the eye and central nervous system.
Bartonella henselae is found worldwide and cat scratch disease has been observed in many countries. The incidence of CSD appears to have a seasonal relationship possibly due to the mating behavior of the cat flea during certain times of the year.
Symptoms similar to Cat scratch disease were first described by Henri Parinaud in 1889 and the clinical syndrome was first described in 1950 by Robert Debré. In 1983, the Warthin-Starry silver stain was used to discover a gram negative bacillus which was named Afipia felis in 1991 after it was successfully cultured and isolated. The causative organism of CSD was originally believed to be Afipia felis, but this was disproved by immunological studies in the 1990s demonstrating that cat scratch fever patients developed antibodies to two other organisms, Bartonella henselae (originally known as Rochalimea henselae before the genera Bartonella and Rochalimea were combined) and Bartonella clarridgeiae, which are rod-shaped Gram-negative bacteria.
- Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- Florin TA, Zaoutis TE, Zaoutis LB (2008). "Beyond cat scratch disease: widening spectrum of Bartonella henselae infection". Pediatrics 121 (5): e1413–25. doi:10.1542/peds.2007-1897. PMID 18443019.
- Klotz SA, Ianas V, Elliott SP (January 2011). "Cat-scratch Disease". Am Fam Physician 83 (2): 152–5. PMID 21243990.
- Asano S (2012). "Granulomatous lymphadenitis". J Clin Exp Hematop 52 (1): 1–16. PMID 22706525.
- "Catscratch disease: Clinical presentations". Emedicine. Retrieved 11 September 2012.
- Perkocha LA, Geaghan SM, Yen TS et al. (December 1990). "Clinical and pathological features of bacillary peliosis hepatis in association with human immunodeficiency virus infection". N. Engl. J. Med. 323 (23): 1581–6. doi:10.1056/NEJM199012063232302. PMID 2233946.
- Higgins JA, Radulovic S, Jaworski DC, Azad AF (May 1996). "Acquisition of the cat scratch disease agent Bartonella henselae by cat fleas (Siphonaptera:Pulicidae)". J. Med. Entomol. 33 (3): 490–5. PMID 8667399.
- Foil L, Andress E, Freeland RL et al. (September 1998). "Experimental infection of domestic cats with Bartonella henselae by inoculation of Ctenocephalides felis (Siphonaptera: Pulicidae) feces". J. Med. Entomol. 35 (5): 625–8. PMID 9775583.
- Nunes Rosado, Flavia G.; Stratton, Charles W.; Mosse, Claudio A. (2011). "Clinicopathologic Correlation of Epidemiologic and Histopathologic Features of Pediatric Bacterial Lymphadenitis". Archives of Pathology & Laboratory Medicine 135 (11): 1490–3. doi:10.5858/arpa.2010-0581-OA. PMID 22032579.
- "Catscratch disease: Treatment and management". E-medicine. Retrieved 11 September 2012.
- CDC information
- DermNet bacterial/catscratch
- Cat Scratch Disease on National Organization for Rare Disorders site
- Cat Scratch Fever Disease