Oral submucous fibrosis secondary to iron deficiency anemia: A case report, etiopathogenesis and management

2015 ◽  
Vol 20 (2) ◽  
pp. 205-208 ◽  
Author(s):  
Preeti Tomar Bhattacharya ◽  
T. Khaitan ◽  
S. B. Sarkar ◽  
R. Sinha
Keyword(s):  
Case Report ◽  
Iron Deficiency ◽  
Iron Deficiency Anemia ◽  
Oral Submucous Fibrosis ◽  
Deficiency Anemia ◽  
Submucous Fibrosis

scholarly journals Iron Deficiency Anemia in Oral Submucous Fibrosis

2018 ◽  
Vol 2 (2) ◽  
pp. 51-54 ◽  
Author(s):  
Richa Saxena ◽  
Monisha Batra
Keyword(s):  
Iron Deficiency ◽  
Iron Deficiency Anemia ◽  
Oral Submucous Fibrosis ◽  
Deficiency Anemia ◽  
Submucous Fibrosis

Case report of severe iron deficiency anemia caused by proton pump inhibitor in an elderly patient

2017 ◽  
Vol 17 (4) ◽  
pp. 662-663 ◽  
Author(s):  
Suguru Mabuchi ◽  
Risa Suzuki ◽  
Mari Sasaki ◽  
Marie Nakamura ◽  
Norihiko Izumimoto ◽  
...  
Keyword(s):  
Elderly Patient ◽  
Case Report ◽  
Iron Deficiency ◽  
Proton Pump Inhibitor ◽  
Iron Deficiency Anemia ◽  
Proton Pump ◽  
Deficiency Anemia

scholarly journals Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Peng Yong Sim ◽  
Priyal Taribagil ◽  
Ione O. C. Woollacott ◽  
Safina Rashid ◽  
Desmond P. Kidd
Keyword(s):  
Case Report ◽  
Iron Deficiency ◽  
Intracranial Hypertension ◽  
Iron Deficiency Anemia ◽  
Idiopathic Intracranial Hypertension ◽  
Deficiency Anemia ◽  
Visual Deficits ◽  
Fluid Analysis ◽  
Optic Disc Swelling

Abstract Background The presentation of idiopathic intracranial hypertension (IIH) in association with iron deficiency anemia (IDA) is rare. Case presentation This case report depicts the unusual case of a 31-year-old woman of mixed Jamaican and English heritage with IIH who presented initially as IDA in the context of menorrhagia. Subsequent ophthalmic review, lumbar puncture, cerebrospinal fluid analysis and neuroimaging studies revealed severe bilateral optic disc swelling and raised intracranial pressure in keeping with IIH. Prompt treatment of IDA with blood transfusion and orally administered iron supplements, in addition to medical treatment for IIH, contributed to significant improvement of symptoms and prevented long-term visual deficits. Conclusion The possibility of IDA, albeit rare, should always be considered and investigated appropriately in all patients with IIH, as the treatment of the anemia alone may be sight-saving.

Pica and iron-deficiency anemia: A case report

1992 ◽  
Vol 50 (6) ◽  
pp. 633-635 ◽  
Author(s):  
Daniel G. Loggi ◽  
Glenn R. Regenye ◽  
Maano Milles
Keyword(s):  
Case Report ◽  
Iron Deficiency ◽  
Iron Deficiency Anemia ◽  
Deficiency Anemia

scholarly journals A Rare Case Report on Plummer-Vinson Syndrome with a Complication of Oral Cancer in a South-Asian Woman

2020 ◽  
Vol 14 (1) ◽  
Author(s):  
Ayisha Ayisha ◽  
Sheema Masood Ali
Keyword(s):  
Squamous Cell Carcinoma ◽  
Case Report ◽  
Iron Deficiency ◽  
Cell Carcinoma ◽  
Iron Deficiency Anemia ◽  
Squamous Cell ◽  
Whole Body ◽  
Deficiency Anemia ◽  
Plummer Vinson Syndrome ◽  
Increased Risk

Plummer-Vinson syndrome (PVS), also called "Paterson-Brown-Kelly syndrome“, is a rare medical syndrome generally affecting middle-aged women. Iron deficiency anemia is the prime etiological factor and other probable factors include malnutrition, genetic predisposition, or autoimmune processes characterized by three distinctive features: iron deficiency anemia, dysphagia, and esophageal web. The dysphagia is generally painless and intermittent or progressive over years, restricted to solids, and associated with weight loss. The exact pathogenesis of PVS is still indistinguishable, but it is interconnected with iron deficiency anemia. Plummer-Vinson syndrome, if left untreated, carries an increased risk of developing squamous cell carcinoma of the upper alimentary tract.In this case report, a 40-year-old female patient presented long-standing dysphagia for months, which progressively developed to postcricoid squamous cell carcinoma by the time she approached to medical treatment. Diagnosis was confirmed through laboratory tests, showing iron deficiency anemia and whole-body positron emission tomography-computed tomography (PET-CT) presenting squamous cell carcinoma in postcricoid region (hypopharynx).

scholarly journals SEVERE IRON DEFICIENCY ANEMIA IN AN INFANT: A CASE REPORT

2017 ◽  
Vol 04 (03) ◽  
pp. 449-450
Author(s):  
Archana Agrawal ◽  
Piyush Chaudhary ◽  
Prabjyot Singh
Keyword(s):  
Case Report ◽  
Iron Deficiency ◽  
Iron Deficiency Anemia ◽  
Deficiency Anemia
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