Systemic autoimmune disorders associated with celiac disease (CD): a case report

We read with deep attention the case report recently published about the peculiar association of morphea, celiac disease, dermatitis herpetiformis and dermatomyositis , and we would discuss the particular genetics that lay behind morphea and related autoimmune disorders, with a focus on HLA genes.

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An unique case of celiac disease with hypocoagulation and secondary hyperparathyreodism in elderly patient - a case report

Endocrine Abstracts ◽

10.1530/endoabs.49.ep315 ◽

2017 ◽

Author(s):

Gocha Barbakadze ◽

Lali Tigishvili ◽

Levan Ramishvili ◽

Nani Tsikarishvili ◽

Koba Burnadze

Keyword(s):

Elderly Patient ◽

Celiac Disease ◽

Case Report ◽

Unique Case

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CHRONIC URTICARIA AND CELIAC DISEASE IN A CHILD: A CASE REPORT Chronic urticaria and celiac disease in a child: A case report

10.26226/morressier.5acc8ad5d462b8028d89b26c ◽

2018 ◽

Author(s):

PASCHALINI TSEKLAZI

Keyword(s):

Celiac Disease ◽

Case Report ◽

Chronic Urticaria

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Case Report: Papillary Thyroid Cancer in a Patient with Celiac Disease and Thalassemia Trait

Case Reports in Oncology ◽

10.1159/000511068 ◽

2020 ◽

Vol 13 (3) ◽

pp. 1364-1367

Author(s):

Afaf Albattah ◽

Yahia Imam ◽

Ahmed Osman Saleh ◽

Khalid Ahmed ◽

Tarek Aboursheid ◽

...

Keyword(s):

Risk Factors ◽

Thyroid Cancer ◽

Celiac Disease ◽

Case Report ◽

Papillary Thyroid Cancer ◽

Thalassemia Major ◽

Papillary Thyroid ◽

Unique Case ◽

Thalassemia Trait ◽

Common Risk Factors

Thyroid cancer is the most frequent endocrine neoplasm in the general population. Common risk factors include gender, radiation exposure, and genetic backgrounds. The association of papillary thyroid cancer and celiac disease has frequently been reported in the literature; however, the association of papillary thyroid cancer and thalassemia trait is rare. Likewise, the association of thalassemia major and celiac disease is also rare. We hereby report a unique case of papillary thyroid cancer in a patient with celiac disease and thalassemia trait.

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Esophagitis Dissecans Superficialis (EDS) Secondary to Hair Dye Ingestion: Case Report and Literature Review

Clinics and Practice ◽

10.3390/clinpract11020026 ◽

2021 ◽

Vol 11 (2) ◽

pp. 185-189

Author(s):

Eric Omar Then ◽

Tyler Grantham ◽

Michell Lopez ◽

Madhavi Reddy ◽

Vinaya Gaduputi

Keyword(s):

Case Report ◽

Literature Review ◽

Proton Pump Inhibitors ◽

Proton Pump ◽

Autoimmune Disorders ◽

Pharmacologic Therapy ◽

Esophageal Mucosa ◽

Hair Dye ◽

Esophageal Lesion ◽

Chemical Irritants

Esophagitis dissecans superficialis (EDS) is a rare and underdiagnosed esophageal lesion characterized by sloughing of the esophageal mucosa that has been associated with medications, various autoimmune disorders, and exposure to some chemical irritants. Anatomically, EDS is most commonly seen in the middle and distal thirds of the esophagus. When present, EDS is best treated by discontinuing the offending agent and initiating pharmacologic therapy with proton pump inhibitors. Steroids may also be effective if the etiology is autoimmune in nature. Our case highlights a 65-year-old female diagnosed with EDS after incidental ingestion of hair dye containing resorcinol and para-phenylenediamine (PPD).

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