Background: Prior studies suggested that direct immunofluorescence (DIF) slides can be stored at room temperature.
Objectives: We sought to determine the durability of DIF slides stored at room temperature for 5 years.
Methods: This was a retrospective study of 83 DIF slides archived at room temperature during 2010. The pattern of immunoreactants was compared with those noted in the original report.
Results: Loss of reactivity was limited to cases with weak fluorescence at original diagnosis. Loss of IgG was noted in 12.5% of cases, IgA in 12%, C3 in 10%, and IgM in 9.75%. Fibrin showed no loss of reactivity. Preservation of immunofluorescence was not related to site of deposition. Overall, a reliable diagnosis could be made in 75 of 79 archived cases (94.9%).
Limitations: Cases had been archived for periods varying from 4.5 to 5 years. Variations in processing and fluorochromes could affect durability. We have no way of knowing how long slides had been exposed to ultraviolet light at the time of initial examination.
Conclusion: DIF showed excellent durability in slides kept at room temperature for 5 years.
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http://dx.doi.org/10.1016/j.jaad.2015.07.027 | DOI Listing |
J Cutan Pathol
July 2023
Department of Dermatology, Mayo Clinic, Rochester, Minnesota, USA.
IgA vasculitis is a small-vessel vasculitis subtype with increased risk of systemic involvement. We aimed to investigate if any light-microscopic features can predict the presence of perivascular granular IgA deposits on direct immunofluorescence (DIF) microscopy. We performed a retrospective search of cutaneous pathology reports from our internal and consultation practice (January 1, 2010-October 5, 2021) with a diagnosis of leukocytoclastic vasculitis and accompanying DIF.
View Article and Find Full Text PDFMicrosc Res Tech
October 2019
Autoimmune Blistering Dermatoses Section, Department of Dermatology, Poznan University of Medical Sciences, Poznan, Poland.
Direct immunofluorescence (DIF) microscopy still is the gold standard in diagnosing and differentiating subepidermal autoimmune blistering diseases (SABDs) from other bullous diseases. New optical systems were developed that aim to facilitate DIF images evaluation. The aim of the study was to evaluate the usefulness of three fluorescence microscopy systems with different light source for routine diagnostics of SABDs with DIF.
View Article and Find Full Text PDFJ Am Acad Dermatol
December 2015
Ackerman Academy of Dermatopathology, New York, New York. Electronic address:
Background: Prior studies suggested that direct immunofluorescence (DIF) slides can be stored at room temperature.
Objectives: We sought to determine the durability of DIF slides stored at room temperature for 5 years.
Methods: This was a retrospective study of 83 DIF slides archived at room temperature during 2010.
Rev Bras Parasitol Vet
May 2012
Faculdade de Medicina Veterinária, Universidade Estadual Paulista, Araçatuba, SP, Brazil.
The aim of this study was to produce a conjugate containing anti-Cryptosporidium parvum polyclonal antibodies and standardize a Direct Immunofluorescence Assay (DIF) for detecting C. parvum oocysts in fecal samples from calves. In order to obtain anti-C.
View Article and Find Full Text PDFClin Exp Dermatol
April 2011
Department of Dermatology, PSG Institute of Medical Sciences and Research, Peelamedu, Coimbatore, India.
Background: The direct immunofluorescence (DIF) pattern of the outer root sheath (ORS) of the hair follicle in patients with pemphigus resembles that of perilesional skin. We performed DIF on anagen and telogen hair ORS from patients with pemphigus and compared the findings with those of perilesional skin.
Aim: To assess the sensitivity of DIF in the ORS of anagen and telogen hair in patients with pemphigus with positive DIF results in perilesional skin.
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