Autoerythrocyte sensitization syndrome with positive anticardiolipin antibodies

Sudy,; Urbina,; Vásquez,

doi:10.1046/j.1365-2133.1998.02102.x

Cited by 18 publications

(15 citation statements)

References 7 publications

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“…Ce syndrome n'est pas classé parmi les maladies immuno-inflammatoires car les biopsies cutanées ne montrent pas de signes inflammatoires. Les signes histologiques consistent en un oedème du derme, une extravasation des érythrocytes et des infiltrats aigus inflammatoires périvasculaires [8,10].…”

Section: Discussionunclassified

“…Le syndrome de Gardner-Diamond a été décrit en association avec certaines maladies auto-immunes ou inflammatoires [4][5][6][7][8] : lupus érythémateux disséminé [4], néphrite à complexes immuns [5], hypocomplémentémie [6], purpura thrombopénique idiopathique [7], adénopathie angio-immunoplastique [6] et présence d'anticorps anticardiolipine [8]. Ratnoff a décrit les lésions du syndrome de Gardner-Diamond comme des ecchymoses inflammatoires [2].…”

Section: Discussionunclassified

“…* Bien que le syndrome de Gardner-Diamond ne soit pas classé parmi les affections auto-inflammatoires, on peut y observer des signes immuno-inflammatoires [4][5][6][7][8]. Nous décrivons une observation de vascularite cutanée chez une femme qui avait un syndrome de Gardner-Diamond et nous passons brièvement en revue les signes inflammatoires qui peuvent accompagner cette affection.…”

Section: Introductionunclassified

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Autosensibilisation aux érythrocytes (syndrome de Gardner-Diamond) associée à une vascularite cutanée

Kaşifoğlu

Paşaoğlu

Korkmaz

2008

Revue du Rhumatisme

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Section: Discussionunclassified

Section: Introductionunclassified

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Autosensibilisation aux érythrocytes (syndrome de Gardner-Diamond) associée à une vascularite cutanée

Kaşifoğlu

Paşaoğlu

Korkmaz

2008

Revue du Rhumatisme

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“…5,7 A number of other dysregulations have been postulated as the underlying pathomechanism of GDS in a minority of reported cases, such as alterations in the fibrinolytic pathway, coexisting coagulation or bleeding disorders and the presence of anticardiolipin antibodies or systemic lupus erythematosus. [8][9][10] Our case demonstrated typical GDS followed by IMS and emotional stress. We were unable to detect any relationships between each episode and menstrual, immunological or hematological abnormalities.…”

Section: Case Of Gardner-diamond Syndrome After Intramuscular Stimulamentioning

confidence: 99%

An extreme and unusual variant of Ramsay Hunt syndrome

Pfleiderer

1999

J. Laryngol. Otol.

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have communicating branches, by which the VZV could involve multiple cranial nerves. 8 Inflammation and edema of the multiple nerves might play a major role in the course of Ramsay-Hunt syndrome. These might be the reasons for the patient's multiple cranial nerve involvement. Due to the early application of antiviral agents and glucocorticosteroid, or a younger age or the acupuncture and infrared physiotherapy, he recovered faster than many cases in the published work. REFERENCES 1 Hunt JR. On herpetic inflammations of the geniculate ganglion. A new syndrome and its complications. J Nerve Ment Dis 1907; 34 (2): 73-96. 2 Asnis DS, Micic L, Giaccio D. Ramsay Hunt syndrome isherpes zoster of the facial nerve, frequently associated with VIII cranial nerve involvement, but on rare occasions V, VI, IX, and X cranial nerves are affected as well. We present a case of a Ramsay Hunt syndrome with involvement of V, VII, and VIII cranial nerves.

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“…However, the effects of psychotherapy or antidepressants were variable 5,7 . A number of other dysregulations have been postulated as the underlying pathomechanism of GDS in a minority of reported cases, such as alterations in the fibrinolytic pathway, coexisting coagulation or bleeding disorders and the presence of anticardiolipin antibodies or systemic lupus erythematosus 8–10 …”

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confidence: 99%