Iron deficiency koilonychia
Specialty: Hematology.
Why it occurs
- Chronic and severe iron deficiency anemia (prolonged depletion of the body's iron stores alters the enzymes that contain this metal, such as cellular cytochromes and ribonucleotide reductase, weakening the keratinization of the nail matrix)
- Hereditary hemochromatosis (paradox of tissue accumulation of iron that deforms the structure of the nail due to deposition and local dysfunction)
- Plummer-Vinson/Paterson-Kelly syndrome (classic triad of severe iron deficiency anemia, esophageal webbing, and glossitis/koilonychia)
- Celiac disease or other chronic intestinal malabsorption syndromes (such as gastric or duodenal resection, which prevent adequate absorption of non-heme iron)
- Chronic exposure to petroleum-based industrial solvents or repetitive microtrauma of occupational origin.
Initial workup
Complete blood count with detailed erythrocyte indices (mean corpuscular volume - decreased MCV, mean corpuscular hemoglobin - decreased HCM, erythrocyte distribution amplitude - elevated RDW, confirming cellular heterogeneity or anisocytosis); comprehensive serum iron profile (serum iron determination, decreased serum ferritin typically <15-30 ng/mL, increased total iron binding capacity - TIBC and percent transferrin saturation less than 15%); peripheral blood smear to demonstrate microcytosis, marked hypochromia, elliptocytes and target cells; upper gastrointestinal endoscopy and colonoscopy (mandatory in men and postmenopausal women to identify the focus of gastrointestinal blood loss); screening for celiac disease using anti-tissue transglutaminase IgA antibodies and total serum IgA levels.
red flags
Coexistence with progressive dysphagia, initially for solids, associated with food impaction (highly suggestive of the development of postcricoid esophageal membranes in the context of Plummer-Vinson syndrome, a pathology with increased risk of progression to squamous cell carcinoma of the esophagus); hematochezia, melena or involuntary and progressive weight loss (which point to digestive bleeding of tumor or organic origin as a cause of the underlying iron deficiency); dyspnea on minimal exertion, orthopnea or chest pain with anginal characteristics secondary to severe anemia with hemodynamic repercussions.
Standard management
- Sulfato ferroso — first choice oral supplement; provides 60-65 mg of elemental iron for each 200-325 mg tablet; It is preferably administered on an empty stomach and spaced from antacids or dairy products, and may be accompanied by ascorbic acid to improve gastrointestinal absorption; causes frequent adverse effects such as heartburn, constipation and darkening of stools
- Iron carboxymaltose — intravenous iron formulation, indicated for therapeutic failure or intolerable intolerance to oral iron, active malabsorption syndromes such as inflammatory bowel disease, or severe, rapidly evolving iron deficiency anemia
- Iron hydroxide and polymaltose complex — oral iron alternative with a lower incidence of gastrointestinal adverse effects due to its slower and more controlled release
- Ascorbic acid / Vitamin C (oral adjuvant supplement to promote the reduction of iron from its ferric to ferrous state, facilitating its transport through enterocytes).
Educational guidance for study. It is NOT a prescription recommendation. The actual choice depends on the cause, the patient, and current guidelines.
- Area
- Hematology
- Listed causes
- 5
- Treatment options
- 4