Papular acantholytic dyskeratosis of the anogenital area with positive direct immunofluorescence results

2007 ◽  
Vol 32 (3) ◽  
pp. 301-303 ◽  
Author(s):  
A. T. Güneş ◽  
T. Ilknur ◽  
U. Pabuççuoğlu ◽  
B. Lebe ◽  
D. D. Altiner
2008 ◽  
Vol 35 (8) ◽  
pp. 508-513 ◽  
Author(s):  
Patcharin JANJUMRATSANG ◽  
Daraka PHAINUPONG ◽  
Somchai CHANJANAKIJSKUL ◽  
Paisal ROONGPHIBULSOPIT

2021 ◽  
Vol 12 ◽  
Author(s):  
Hua Qian ◽  
Yohei Natsuaki ◽  
Hiroshi Koga ◽  
Tamihiro Kawakami ◽  
Chiharu Tateishi ◽  
...  

BackgroundRecently, we published an article retrospectively summarizing the results in 55 anti-laminin 332 (LM332)-type mucous membrane pemphigoid (MMP) cases examined at Kurume University, which were diagnosed by strict inclusion criteria, including positive reactivity in direct immunofluorescence and absence of antibodies to non-LM332 autoantigens. However, indirect immunofluorescence using 1M-NaCl-split normal human skin (ssIIF) is also valuable for diagnosis of anti-LM332-type MMP.MethodsIn this second study, we selected 133 anti-LM332-type MMP cases, which were diagnosed by our different inclusion criteria: (i) immunoglobulin G (IgG) deposition to basement membrane zone (BMZ) by direct immunofluorescence or IgG reactivity with dermal side of split skin by ssIIF, (ii) positivity for at least one of the three subunits of LM332 by immunoblotting of purified human LM332, and (iii) the presence of mucosal lesions. Clinical, histopathological, and immunological findings were summarized and analyzed statistically. Although these cases included the 55 previous cases, the more detailed study for larger scale of patients was conducted for further characterization.ResultsClinically, among the 133 patients, 89% and 43% patients had oral and ocular mucosal lesions, respectively, 71% had cutaneous lesions, and 17% had associated malignancies. Histopathologically, 93% patients showed subepidermal blisters. The sensitivities of ssIIF and direct immunofluorescence are similar but are significantly higher than indirect immunofluorescence using non-split human skin (both p < 0.001). In immunoblotting of purified LM332, patient IgG antibodies most frequently reacted with LMγ2 subunit (58%), followed by LMα3 (49%) and LMβ3 (36%). Thirty-four percent patients recognized additional non-LM332 autoantigens. Statistical analysis revealed that autoantibodies against non-LM332 autoantigens might stimulate the production of anti-LMγ2 antibodies.ConclusionsThis retrospective study further characterized in more detail the clinical and immunological features of 133 cases of anti-LM332-type MMP, in which the new diagnostic criteria without positive direct immunofluorescence reactivity were useful for the diagnosis. Higher frequency with anti-LMγ2 antibodies suggested more significant pathogenic role of this subunit. Additional autoantibodies to non-LM332 autoantigens detected in one-third of the patients may contribute to complexity in anti-LM332-type MMP, including the induction of anti-LMγ2 antibodies.


2021 ◽  
Vol 134 (12) ◽  
pp. 1508-1510
Author(s):  
Xue-Min Xiao ◽  
Yi-Qun Jiang ◽  
Wei Tian ◽  
Cheng-Rang Li

2019 ◽  
Vol 12 (10) ◽  
pp. e231152
Author(s):  
Luís Santiago ◽  
Rosa Mascarenhas ◽  
Óscar Tellechea ◽  
Margarida Gonçalo

Specific vesiculobullous skin lesions in lupus erythematosus (LE) are rare and must be differentiated from toxic epidermal necrolysis (TEN), TEN-like dermatoses and other vesiculobullous conditions. We report a patient with typical subacute cutaneous lupus erythematous that progressed with large sheet-like areas of epidermal detachment and Nikolsky sign resembling TEN. She had a serological profile suggestive of underlying connective tissue disease, histological findings of interface dermatitis with a lymphocytic infiltrate, positive direct immunofluorescence, resolution with immunomodulation and lack of a culprit drug, features observed in TEN-like cutaneous lupus erythematous. Furthermore, she was diagnosed with lung carcinoma, an association that has been previously reported. Differentiating a bullous eruption in the context of pre-existing LE remains difficult requiring a thorough analysis of clinical and histopathological data.


Sign in / Sign up

Export Citation Format

Share Document