- Case report
- Open Access
Pica and refractory iron deficiency anaemia: a case report
Journal of Medical Case Reports volume 2, Article number: 324 (2008)
Iron deficiency is the most common cause of anaemia worldwide. Pica, the ingestion of substances that are inappropriate for consumption, is associated with iron deficiency and may be under-diagnosed.
A 34-year-old woman presented with iron deficiency anaemia refractory to treatment for more than a decade. The clinical presentation, endoscopic findings and laboratory investigations were consistent with pica. Subsequent geophysical analysis confirmed that the ingested material was kaolin, a negatively charged silicate.
Prolonged unexplained iron deficiency anaemia should prompt clinicians to remember and inquire about pica. In our patient, this would have averted numerous unnecessary investigations and prevented a decade-long suffering.
Pica refers to an ill-defined entity known as a perverted appetite for substances inappropriate for consumption, such as kaolin (geophagia) . Cultural factors may influence this dietary behaviour, which can even lead to serious complications that require surgical intervention [2, 3]. Kaolinite is the most important component of kaolin, a white chalky silicate used in the paper-coating industry, in ceramics production and in the pharmaceutical industry. The negatively charged surface of kaolinite is able to exchange and adsorb cations (for example, Fe2+ and Fe3+) in the duodenum, where iron absorption occurs. As a consequence, iron deficiency anaemia may be associated with the ingestion of kaolin. We report the case of an African woman who had lived in Europe for more than a decade and presented with a 12-year history of seemingly refractory iron deficiency anaemia.
A 22-year-old African woman first presented to our medical outpatients department in 1993 with anaemia, with test results as follows: haemoglobin (Hb) 96 g/litre (normal range 120 to 160 g/litre), mean corpuscular volume (MCV) 74.7 fl (normal range 79 to 95 fl), mean corpuscular haemoglobin concentration (MCHC) 313 g/litre (normal range 320 to 360 g/litre), reticulocytes 13‰ (normal range 5 to15‰) and ferritin of 9 ng/ml (normal range 10 to 200 ng/ml). Iron deficiency was the most likely cause, but further investigations (occult stool blood test, gastroscopy, colonoscopy, gynaecological examination, Hb electrophoresis) failed to show an obvious bleeding source or abnormal Hb. Despite oral iron replacement therapy (160 mg of Fe2+ daily), Hb values remained low (100 to 115 g/litre) over the next 4 years, after which the patient was lost to follow-up.
Twelve years later, in 2005, the patient presented with incapacitating fatigue related to severe iron deficiency anaemia (Hb 75 g/litre, MCV 64.6 fl, MCHC 299 g/litre, reticulocytes 13‰, ferritin 6 ng/ml and soluble transferrin receptor 13.4 mg/ml (normal range 2.2 to 4.5 mg/ml)). Gastroscopy showed normal gastric mucosa and histological evidence of a highly active gastritis with Helicobacter pylori infestation in biopsy samples. A capsule endoscopy revealed several non-specific erythematous mucosal changes in the bulbus duodeni not seen during gastroscopy.
During a follow-up visit and further explicit questioning about particular eating habits, the patient reluctantly disclosed an almost daily consumption of 'a friable stone' over more than a decade. She reported having developed a particularly strong craving for such stones, of which she would suck on small pieces until these completely dissolved. She had acquired this habit 15 years ago in her home country Cameroon, where consumption of stones is common. To characterise the chalky stone (Figure 1), we contacted our geosciences department. X-ray diffraction measurements confirmed that the substance was essentially composed of kaolinite with traces of quartz (Figure 2). After cessation of kaolinite ingestion, we administered intravenous iron replacement therapy (total of 1000 mg) and the anaemia was corrected within 1 month (Hb 125 g/litre, MCV 79.4 fl, MCHC 333 g/litre, ferritin 13 ng/ml, soluble transferrin receptor 6.6 mg/ml). Tests 3 months later showed a stable blood count and iron studies as follows: Hb 120 g/litre, MCV 83.6 fl, MCHC 346 g/litre, ferritin 11 ng/ml and soluble transferrin receptor 6.0 mg/ml.
The word pica comes from the Latin word for magpie, a bird known for its unusual eating habits. Pica is characterised by persistent craving and compulsive eating of non-food substances. Pica in humans has many different subgroups, defined by the substance that is ingested. Examples of pica are eating earth, soil or clay (geophagia) or ice (pagophagia). The prevalence and type of pica depend on ethnic and cultural factors that affect dietary practices . Pica has been reported to be associated with severe iron deficiency anaemia in up to half of patients; however, it is unclear whether pica causes or is the consequence of iron deficiency anaemia [5–8]. In our case, there are several reasons why kaolin ingestion may have caused iron deficiency anaemia. First, experimental data from kaolin-fed pregnant rats showed significant maternal anaemia and reduced birth weight, both of which were prevented in the iron-supplementation control group . Second, adsorption of Fe2+ and Fe3+ to the negatively charged and large active surface area of kaolinite may lead to a reduction of available iron in the duodenum. As a consequence, the absorption of iron might decrease, resulting in iron deficiency. Third, traces of quartz commonly found in kaolinite may cause abrasion and favour increased mucosal sloughing and iron loss. Fourth, kaolin consumption and geophagia may cause parasitic infestation and further iron loss [7–10].
Although pica is a rare condition in central Europe , it may be underestimated in multicultural societies and it is therefore important to remember and inquire about particular eating habits in the context of unexplained iron deficiency anaemia. Thus, proper history remains the most inexpensive investigation.
In the context of an unexplained iron deficiency anaemia, it is important to remember and inquire about pica. In our patient, this would have averted numerous unnecessary investigations and prevented a decade of suffering.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
mean corpuscular haemoglobin concentration
mean corpuscular volume.
Lacey EP: Broadening the perspective of pica: literature review. Public Health Rep. 1990, 105: 29-35.
Anderson JE, Akmal M, Kittur DS: Surgical complications of pica: report of a case of intestinal obstruction and a review of the literature. Am Surg. 1991, 57: 663-667.
Grigsby RK, Thyer BA, Waller RJ, Johnston GA: Chalk eating in middle Georgia: a culture-bound syndrome of pica?. South Med J. 1999, 92: 190-192. 10.1097/00007611-199902000-00005.
Simpson E, Mull JD, Longley E, East J: Pica during pregnancy in low-income women born in Mexico. West J Med. 2000, 173: 20-24. 10.1136/ewjm.173.1.20.
Coltman CA: Pagophagia and iron lack. Nutr Rev. 1969, 27: 244-
Crosby WH: Food pica and iron deficiency. Arch Intern Med. 1971, 127: 960-961. 10.1001/archinte.127.5.960.
Geissler PW, Mwaniki DL, Thiong'o F, Michaelsen KF, Friis H: Geophagy, iron status and anaemia among primary school children in Western Kenya. Trop Med Int Health. 1998, 3: 529-534. 10.1046/j.1365-3156.1998.00272.x.
Lanzkowsky P: Investigation into the aetiology and treatment of pica. Arch Dis Child. 1959, 34: 140-148.
Patterson EC, Staszak DJ: Effects of geophagia (kaolin ingestion) on the maternal blood and embryonic development in the pregnant rat. J Nutr. 1977, 107: 2020-2025.
Geissler PW, Mwaniki D, Thiong F, Friis H: Geophagy as a risk factor for geohelminth infections: a longitudinal study of Kenyan primary schoolchildren. Trans R Soc Trop Med Hyg. 1998, 92: 7-11. 10.1016/S0035-9203(98)90934-8.
Schnuelle P, Oberheiden T, Hohenadel D, Gottmann U, Benck U, Nebe T, Krammer HJ, Woude van der FJ, Birck R: An unusual case of severe iron deficiency anaemia. Gut. 2006, 55: 1060-10.1136/gut.2006.094680.
We thank Daniel Boller, Gastroenterology Division, Basel University Hospital, for performing and interpreting the gastroscopy, colonoscopy and capsule endoscopy.
The authors declare that they have no competing interests.
CVG managed the patient, conceived the initial idea and drafted the paper. HS performed and interpreted the geophysical investigations. MD reviewed and interpreted the full blood counts and iron studies. EB critically reviewed and interpreted the investigations. AZ managed the patient and critically reviewed the manuscript. All authors read and approved the final manuscript.
About this article
Cite this article
von Garnier, C., Stünitz, H., Decker, M. et al. Pica and refractory iron deficiency anaemia: a case report. J Med Case Reports 2, 324 (2008). https://doi.org/10.1186/1752-1947-2-324
- Iron Deficiency
- Iron Deficiency Anaemia
- Mean Corpuscular Volume