EPONYMS LINKED TO VACCINES AND ITS REACTIONS
Khalid Al Aboud1, Daifullah Al Aboud2
Corresponding author: Dr. Khalid Al Aboud e-mail: amoa65@hotmail.com
How to cite an article: Al Aboud K, Al Aboud D. Eponyms linked to vaccines and its reactions. Our Dermatol Online. 2013; 4(4): 559-563.
Eponyms linked to vaccines and its
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Remarks
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BCG [3-5] |
Bacillus Calmette–Guérin (Historically Vaccin Bilié de Calmette et Guérin commonly referred as Bacille de Calmette et Guérin or BCG) is a vaccine against tuberculosis that is prepared from a strain of the attenuated live bovine tuberculosis bacillus, Mycobacterium bovis. It is named for, Léon Charles Albert Calmette (1863-1933), (Fig. 1), who was a French physician, bacteriologist and immunologist and Jean-Marie Camille Guérin (1872–1961), (Fig. 2), who was a French veterinarian, bacteriologist and immunologist.
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Brown-Séquard syndrome [6,7]
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Also known as Brown-Séquard’s hemiplegia and Brown-Séquard’s paralysis, is a loss of
sensation and motor function that is caused by the lateral hemisection of the spinal cord. It was first described in 1850 by the famed British / Mauritian neurologist Charles-Édouard Brown-Séquard (1817–1896), (Fig. 3), who studied the anatomy and physiology of the spinal cord. He described this injury after observing spinal cord trauma happen to farmers while cutting sugar cane in Mauritius. Transverse myelitis with Brown-Séquard syndrome following a prophylactic influenza vaccination has been reported.
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Dravet syndrome [8]
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Also known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a rare and catastrophic form of intractable epilepsy that begins in infancy. Vaccination might trigger earlier onset of Dravet syndrome in children who, because of an SCN1A mutation, are destined to develop the disease. Dravet syndrome has been found recently as an important underlying condition in cases of alleged vaccine encephalopathy after pertussis vaccination, where vaccination seemed to have precipitated the occurrence of the disease without modifying the long-term course. Dravet syndrome was first described by French physician, Dr. Charlotte Dravet, (Fig. 4), in 1978.
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Evans syndrome [9]
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Evans syndrome is an autoimmune disease in which an individual’s antibodies attack their own red blood cells and platelets. The syndrome was first described in 1951 by R. S. Evans and colleagues. It has been reported to be occur after vaccination.
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Gianotti-Crosti syndrome [10]
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Also known as papular acrodermatitis of childhood. Documented to follow several vaccines. It is named for Ferdinando Gianotti (1920-1984),who was an Italian physician and Agostino Crosti Agostino Crosti (1896-1988), who was an Italian dermatologist. | ||||||
Guillain-Barré syndrome [11] |
Guillain–Barré syndrome (GBS) sometimes Landry’s paralysis or Guillain–Barré–Strohl
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Henoch-Schönlein purpura [12,13] |
Also known as, Schönlein–Henoch purpura. It is named for,Eduard Heinrich Henoch (1820– 1910), (Fig.10), a German pediatrician, and his teacher Johann Lukas Schönlein (1793–1864), (Fig. 11), who described it in the 1860s. This type of vasculitis has been reported to follow vaccination.
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Hughes syndrome [14] |
It is another name for antiphospholipid syndrome, a pro-thrombotic condition was described in 1983 which was characterised by the presence of circulating antiphospholipid antibodies, as well as peripheral thrombosis, a tendency to internal organ involvement, repeated miscarriage, and, occasionally, thrombocytopenia. Named after, Graham Robert Vivian Hughes, (Fig. 12), an English rheumatologist. It is reported to follow vaccination.
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Jenner’s cowpox vaccine [15,16] |
Edward Jenner (1749-1823), (Fig. 13), an English doctor, was the first to study and report on the effects of the use of cowpox vaccination to prevent smallpox.
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Lambert-Eaton myasthenic syndrome ( LEMS) [17,18] |
Also known as, Lambert-Eaton-Rooke syndrome. It is a rare autoimmune disorder that is characterised by muscle weakness of the limbs. Around 60% of those with LEMS have an underlying malignancy. Lambert, Eaton and Rooke at the Mayo Clinic were the first physicians to substantially describe the clinical and electrophysiological findings of the disease in 1956. Lealdes (Lee) McKendree Eaton (1905-1958), an american neurologist, Edward Howard Lambert (1915-2003), (Fig. 14), an american neurophysiologist, and Edward Douglas Rooke (1912-2001), a canadian physician.
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Marjolin’s ulcer [19] |
The term „Marjolin’s ulcer” has been generally accepted to refer to a long-term malignant complication of the scars resulting from burns. However, vaccination, snake bites, osteomyelitis, pilonidal abscesses, pressure sores, and venous stasis may also induce this tumor. It is named after Jean-Nicolas Marjolin (1780 –1850), (Fig. 15), who was a French surgeon and pathologist. It was pointed out that Marjolin did not describe the condition he is eponymously credited with, but that the false ascription to him arose over time.
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Nicolau syndrome [20] |
Nicolau syndrome-also known as Embolia Cutis Medicamentosa-is a rare complication of intramuscular and subcutaneous drug injections manifesting as necrosis of skin and the underlying tissue s. It may follow vaccination. It was first described by Freudenthal in 1924 and Nicolau in 1925 in patients treated for syphilis withbismuth salts. |
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Shoenfeld syndrome [21,22] |
In the 1990s the term „functional somatic syndromes” was applied to several syndromes, including Sick building syndrome (SBS) (a term coined for a set of clinically recognizable symptoms and ailments without a clear cause reported by occupants of a building), multiple chemical sensitivity, repetition stress injury, the side effects of silicone breast implants, the Gulf War syndrome (GWS), chronic fatigue syndrome, the irritable bowel syndrome, and fibromyalgia. Recently, Shoenfeld and Agmon-Levin suggested that four conditionssiliconosis, macrophagic myofascitis, the GWS, and post-vaccination phenomena-which share clinical and pathogenic resemblances, may be included under a common syndrome entitled the „autoimmune (auto-inflammatory) syndrome induced by adjuvants”(ASIA), also known as Shoenfeld’s syndrome. ASIA may also be precipitated by silicon in silicone-filled breast implants (Silicone implant incompatibility syndrome; SIIS). Shoenfeld’s syndrome is named for Yehuda Shoenfeld, M.D., FRCP (Hon). (Fig. 16), the head of Zbludowicz Center for Autoimmune Diseases, Chaim Sheba Medical Center at Tel-Hashomer, who and his team elaborated on the above medical conditions.
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Stevens-Johnson syndrome [23] |
It is a hypersensitivity reaction that affects the skin and the mucous membranes. The main known cause is certain medications, followed by infections and, rarely, cancers. It may also occur after vaccination. It is named for Albert Mason Stevens (1884-1945) and Frank Chambliss Johnson (1894-1934), american pediatricians who jointly published a description of the disorder in the American Journal of Diseases of Children in 1922. |
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Still’s disease [24-27] |
Adult-onset Still’s disease may be precipitated or relapsed after vaccination for hepatitis. In one study no long-term adverse events were reported after influenza vaccination in juvenile idiopathic arthritis (JIA) and control group. Thirty-five percent of children with JIA experienced flare of the disease after vaccination. Protective antibodies against at least 2 vaccine viruses 6 months after vaccination were detected in all patients. Adult-onset Still’s disease is a systemic inflammatory disease. The classic presentation is the triad of persistent high spiking fever, joint pain and a distinctive salmon-colored rash. Still’s disease is named after English physician Sir George Frederic Still (1861-1941), (Fig. 17).
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Table I. Eponyms linked to vaccines and its reactions
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