Evaluation of 41 Cases of Pediatric Granuloma Annulare

July 21, 2022 updated by: Ayse Esra Koku Aksu, Istanbul Training and Research Hospital

Clinical and Histopathological Evaluation of 41 Cases of Pediatric Granuloma Annulare

INTRODUCTION: Granuloma annulare is a non-infectious, granulomatous disease that can affect children and adults. Although there are many studies examining adult patients, there are limited studies examining pediatric granuloma annulare cases. It is aimed to examine the demographic, clinical, and pathological features of pediatric granuloma annulare cases in this study.

MATERIALS and METHODS: This study was performed retrospectively in a single-center, tertiary dermatology hospital. Forty-one patients, under the age of 18 who were admitted to the dermatology outpatient clinic between 2008-2021 and diagnosed with granuloma annulare were scanned from the hospital database and patient photograph archive. Demographic characteristics, and clinical and histopathological features were evaluated.

Study Overview

Status

Completed

Conditions

Detailed Description

Granuloma annulare; is a non-infectious, granulomatous skin reaction with potential triggers that can affect the adult and pediatric age group. Diabetes mellitus, hyperlipidemia, and malignancy have been described in association with adult granuloma annulare cases. While there are studies on the clinical, pathological features and associated diseases in patients with adult granuloma annulare, a limited number of studies have been conducted on pediatric granuloma annulare patients. Therefore, clinical and histopathological evaluation of pediatric granuloma annulare cases was planned in our study.

This study was performed retrospectively in a single-center tertiary dermatology hospital. Patients under the age of 18 who were admitted to the dermatology outpatient clinic between 2008-2021 and diagnosed with granuloma annulare were scanned from the hospital database and patient photograph archive. Cases with uncertain diagnosis were not included in the study. Cases with dermatological findings recorded in detail and/or diagnosed histopathologically were included in the study. Demographic features, lesion localization, lesion characteristics (size, elementary lesion, color), involvement (localized/generalized), histopathological features, concomitant diseases, differential diagnoses in cases with histopathology, regression time and recommended treatments were recorded.

Study Type

Observational

Enrollment (Actual)

41

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey, 34098
        • Istanbul Training and Research Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 18 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients under the age of 18 who were admitted to the dermatology outpatient clinic between 2008-2021 and diagnosed with granuloma annulare

Description

Inclusion Criteria:

  • Being under 18 years old
  • Having granuloma annulare
  • Applying to the Istanbul Training and Research Hospital, Dermatology Outpatient Clinic between 2008-2021
  • Consenting to participate in the study

Exclusion Criteria:

-Being over 18 years old

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Retrospective

Cohorts and Interventions

Group / Cohort
Patients
Patients under the age of 18 who were admitted to the dermatology outpatient clinic between 2008-2021 and diagnosed with granuloma annulare

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of the genders of the pediatric patients with granuloma annulare
Time Frame: day 0
male, female
day 0
Evaluation of the ages of the pediatric patients with granuloma annulare
Time Frame: day 0
age (year)
day 0
Evaluation of the concomitant diseases of the pediatric patients with granuloma annulare
Time Frame: day 0
the concomitant diseases of the participants
day 0
Evaluation of the lesion localization of the pediatric patients with granuloma annulare
Time Frame: day 0
head and neck, upper extremity, lower extremity, trunk
day 0
Evaluation of the lesion duration of the pediatric patients with granuloma annulare
Time Frame: day 0
the time interval in between appearance of the lesion and diagnosis (month)
day 0
Evaluation of the lesion type of the pediatric patients with granuloma annulare
Time Frame: day 0
papule, pustule, plaque, nodule
day 0
Evaluation of the mean size of the lesion
Time Frame: day 0
diameter (cm)
day 0
Evaluation of the clinical involvement
Time Frame: day 0
localized, generalized
day 0
Histopathological evaluation of the infiltration type of the pediatric patients with granuloma annulare
Time Frame: day 0
neutrophilic, lymphocytic, lymphohistiocytic, eosinophil, mixed infiltrations
day 0
Histopathological evaluation of the infiltration pattern of the pediatric patients with granuloma annulare
Time Frame: day 0
Interstitial, palisadic
day 0
Evaluation of epidermal findings
Time Frame: day 0
regular/irregular, hyperkeratosis, acanthosis
day 0
Evaluation of depth of infiltrate
Time Frame: day 0
superficial, medium, deep
day 0

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 11, 2022

Primary Completion (Actual)

May 11, 2022

Study Completion (Actual)

June 1, 2022

Study Registration Dates

First Submitted

July 15, 2022

First Submitted That Met QC Criteria

July 21, 2022

First Posted (Actual)

July 25, 2022

Study Record Updates

Last Update Posted (Actual)

July 25, 2022

Last Update Submitted That Met QC Criteria

July 21, 2022

Last Verified

July 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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