<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">CRCM</journal-id><journal-title-group><journal-title>Case Reports in Clinical Medicine</journal-title></journal-title-group><issn pub-type="epub">2325-7075</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/crcm.2019.87024</article-id><article-id pub-id-type="publisher-id">CRCM-93844</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Recurrent Hypoglycaemia in a Diabetic Patient Presented a Gastric Cancer: Think about Paraneoplastic Syndrome
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ruffin</surname><given-names>Randriamalala</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Lovasoa</surname><given-names>Tika</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mampionona</surname><given-names>Ranaivomanana</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Andriamiarimbola</surname><given-names>Irène Rakotoniaina</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Florine</surname><given-names>Rafaramino</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Andry</surname><given-names>Riel</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Cancerology Department, University Hospital, Fianarantsoa, Madagascar</addr-line></aff><aff id="aff2"><addr-line>Cancerology Department, University Hospital, Antananarivo, Madagascar</addr-line></aff><aff id="aff4"><addr-line>Laboratory Department, University Hospital, Tuléar, Madagascar</addr-line></aff><aff id="aff5"><addr-line>Reanimation Department, University Hospital, Tuléar, Madagascar</addr-line></aff><aff id="aff1"><addr-line>Department of Cancerology and Polyvalent Medicine, University Hospital, Tuléar, Madagascar</addr-line></aff><pub-date pub-type="epub"><day>08</day><month>07</month><year>2019</year></pub-date><volume>08</volume><issue>07</issue><fpage>196</fpage><lpage>203</lpage><history><date date-type="received"><day>26,</day>	<month>April</month>	<year>2019</year></date><date date-type="rev-recd"><day>21,</day>	<month>July</month>	<year>2019</year>	</date><date date-type="accepted"><day>24,</day>	<month>July</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The hypoglycaemia paraneoplastic is uncommon in diabetic patients. Our aim was to report a case of paraneoplastic hypoglycaemia discovered after the diagnosis of gastric adenocarcinoma in a diabetic patient. A 65 years old man, was hospitalized for the management of acute digestive haemorrhage. In his medical history, he had diabetes since 20 years. He was alcoholic weaned for 3 years and had an unexplored repetitive epigastralgia. During his hospitalization, the exploration of acute digestive haemorrhage found a gastric adenocarcinoma with hepatic metastasis. At the 4th day of his hospitalization, he presented a hypoglycaemic coma with capillary blood glucose at 0.36 g/L. The patient was conscious after the infusion of Hypertonic Glucose Solution (HGS) 10%. After 3 days, the recurrent hypoglycaemia occurred and we intermittently treated by infusion of glucose solution 10%. The measurements of insulin level and C-peptide weren’t performed because they didn’t exist in the city. So, the notion of cancer and the recurrent hypoglycaemia even if we stopped the oral antidiabetic therapy make us think of a paraneoplastic syndrome. The chemotherapy associated with corticosteroid therapy is the standard treatment of the hypoglycaemia paraneoplastic but the patient refused the chemotherapy and we couldn’t use the corticosteroid therapy because of digestive haemorrhage. At the end of his hospitalization, he still had hypoglycaemia treated by infusion of glucose solution 10%. In the absence of means of diagnosis, we should think of paraneoplastic syndrome in front of recurrent hypoglycaemia and cancer in the diabetic patient.
 
</p></abstract><kwd-group><kwd>Extrapancreatic Tumors</kwd><kwd> Gastric Carcinoma</kwd><kwd> Hypoglycaemia</kwd><kwd> Paraneoplastic Syndrome</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>In the diabetic patient treated by insulin or hypoglycaemic sulfamide, the hypoglycaemia is one common acute complication but it is rare in the context of paraneoplastic syndrome. The cause of this syndrome is either an insulinoma or extrapancreatic cancers. In the 45% of cases, the extra-pancreatic cancer comes from the mesenchymal tissue in the 45% of cases and rarely, it comes from the epithelial tissue [<xref ref-type="bibr" rid="scirp.93844-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref4">4</xref>] . The paraneoplastic hypoglycaemia is due to the secretion of a precursor of high molecular weight of “Insulin-like Growth Factor-2” (IGF-2) or “big IGF-2”; this precursor mimics the effects of insulin [<xref ref-type="bibr" rid="scirp.93844-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref7">7</xref>] . In the diabetic patients, the causes of hypoglycaemia must be sought to differentiate the reactive hypoglycaemia and the organic hypoglycaemia like the paraneoplastic hypoglycaemia [<xref ref-type="bibr" rid="scirp.93844-ref8">8</xref>] . Indeed, this one can be under diagnosed in case of tumoral pathologies. Sometimes, it is the premature sign of some cancers [<xref ref-type="bibr" rid="scirp.93844-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref11">11</xref>] . Our aim was to report a case of paraneoplastic hypoglycaemia discovered after the diagnosis of gastric adenocarcinoma in the diabetic patient. An informed consent was obtained from the patient to report this case.</p></sec><sec id="s2"><title>2. Case History</title><p>A 65 years old man, state employee retired, was hospitalized at the department of oncology and polyvalent medicine of the University Center Hospital of Antanambao Toliara, in the south of Madagascar for the management of acute digestive haemorrhage.</p><p>In his medical history, he had diabetes since 20 years treated by oral antidiabetic (glibenclamide). His treatment was taken irregularly and was stopped since a few months after a discomfort. He was chronic alcoholic who has been weaned for 3 years. He had a repetition epigastralgia not exploring and a repetition discomfort since a few months. In his eating habits, he took cassava 2 times a day and rice once a day.</p><p>At the admission, he was conscious, his hemodynamic state was stable. His general state was deteriorated and he presented a cutaneo-mucosal pallor. The abdomen was flexible; there was an epigastric pain without portal hypertension signs. There were blackish stools at the digital rectal examination</p><p>He was fasted and his treatment was composed of red blood cell transfusion, plasma transfusion, parenteral alimentation and medicaments to eradicate Helicobacter pylori (amoxicillin, omeprazole, clarythromycin during 14 days).</p><p>After he underwent a digestive endoscopy and we found a bloody bulging mass at the fundus of stomach. We practiced a biopsy of mass and the histological examination found a gastric adenocarcinoma.</p><p>The evolution of digestive haemorrhage was favourable on the 2<sup>nd</sup> day of his admission. So, he begun a semisolid food (soft diet) and we definitively stopped his antidiabetic treatment.</p><p>On the 4th day, the patient presented cold sweats followed by loss of consciousness. The diagnosis of hypoglycaemic coma was immediately withheld, with a capillary blood glucose level of 0.36 g/L.</p><p>An infusion of hypertonic glucose serum 10% instantly normalized its state of consciousness.</p><p>After 3 days, a fasting capillary blood glucose checking revealed hypoglycaemia at 0.42 g/L, confirmed by the plasma glucose measurement. Thus, a discontinuous infusion of GHS 10% was systematically introduced. Despite this, episodes of hypoglycaemia were still observed. <xref ref-type="fig" rid="fig1">Figure 1</xref> shows the kinetics of fasting capillary glycaemia over time during routine infusion of 10% GHS.</p><p>The other blood tests showed a good renal function with a creatinine clearance: 110 mL/min/1.73 m<sup>2</sup> by MDRD formula (Reference value: 120 mL/min/1.73 m<sup>2</sup> +/−20 mL/min/1.73 m<sup>2</sup>); a good hepatic function with AST 30 IU/L (Reference value: 7 - 40 IU/L), ALT 25IU/L (Reference value: 5 - 35 IU/L), GGT 40 IU/L (Reference value: 15 - 55 IU/L), and total bilirubin 8 &#181;mol/L (Reference value: 3 - 22 &#181;mol/L); a microcytic anemia at 9 g/dL (Reference value of hemoglobin: 14 - 18 g/dL) after transfusion of 3 blood bags and a glycated hemoglobin at 6.2% (Reference value: ≤ 7%). Dosages of insulinemia and peptide C were not achieved because of their unavailability.</p><p>Regarding the extension assessment, an abdominal ultrasound showed hepatic nodules suspected of malignancy. The chest X-ray showed no metastases. So, it was therefore stage IV gastric adenocarcinoma. Thus, palliative chemotherapy has been indicated. After the announcement of the diagnosis and prognosis, the patient refused the proposed treatment. We then opted for a best supportive care. At the end of hospitalization, the patient had again presented signs of hypoglycaemia, motivating an outpatient infusion of glucose serums.</p></sec><sec id="s3"><title>3. Discussion</title><p>Numerous studies have been conducted on hypoglycaemia in Madagascar, both in Antananarivo and Toliara. But they are mostly focused on hypoglycaemia caused by alcohol [<xref ref-type="bibr" rid="scirp.93844-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref13">13</xref>] , leaving aside paraneoplastic hypoglycaemia. Alcohol is known to induce immediate hypoglycaemia [<xref ref-type="bibr" rid="scirp.93844-ref14">14</xref>] . Despite the history of chronic alcoholism in our patient, hypoglycaemia of ethyl origin has been ruled out since alcohol has already been weaned since several years.</p><p>Paraneoplastic hypoglycaemia is a rare condition. It is linked to a pancreatic or extrapancreatic tumor. Mesenchymal and hepatic tumours are the most frequently reported in the literature [<xref ref-type="bibr" rid="scirp.93844-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref17">17</xref>] . Those of the digestive tract remain rare [<xref ref-type="bibr" rid="scirp.93844-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref20">20</xref>] . However, the stomach is the most common location in the gastrointestinal tract in 67% of cases [<xref ref-type="bibr" rid="scirp.93844-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref21">21</xref>] . Like our case, a gastric carcinoma is discovered after a digestive bleeding and hypoglycaemia.</p><p>Regarding the circumstances of discovery, to our knowledge there are few studies on the correlation between digestive bleeding and cancer of the digestive tract in Madagascar. A study carried out in the reference center of the Joseph Raseta Befelat&#224;nana University Hospital shows that gastric cancer represents only 2.73% of the causes of upper gastrointestinal bleeding. These are mainly related to duodenal ulcer, which accounts for 31.50% of cases [<xref ref-type="bibr" rid="scirp.93844-ref22">22</xref>] . Some atypical cases of digestive cancers have also been reported [<xref ref-type="bibr" rid="scirp.93844-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref24">24</xref>] . Gastric adenocarcinoma frequently affects men, aged 60 and over, smoking and having a history of Helicobacter pylori infection. Digestive haemorrhage is manifested in the majority of cases in the advanced stage of the disease [<xref ref-type="bibr" rid="scirp.93844-ref25">25</xref>] . Our patient with melena was diagnosed with metastatic gastric adenocarcinoma. So, we should explore every digestive bleeding to seeking a cancer cause like a gastric cancer.</p><p>The hypoglycaemia is the most common acute complication of diabetes. It is most often of iatrogenic origin [<xref ref-type="bibr" rid="scirp.93844-ref26">26</xref>] . The sulfamids are the most incriminated. In fact, the risk of hypoglycaemia due to their use is related to their plasma half-life and their binding to their receptors. For glibenclamide, still widely used in Africa but less and less in developed countries [<xref ref-type="bibr" rid="scirp.93844-ref27">27</xref>] , its half-life is 4 to 11 hours and its binding to its receptors is strong and durable, explaining the frequent occurrence of hypoglycaemia. The hypoglycaemia is more frequent and severe in the elderly and/or with renal insufficiency [<xref ref-type="bibr" rid="scirp.93844-ref28">28</xref>] . Our patient took glibenclamide but already stopped for several months before his hospitalization. So, the cause of his hypoglycaemia has no relation with the drug intake. A study carried out on diabetic patients admitted for severe hypoglycaemia in the Joseph Raseta Befelat&#224;nana University Hospital shows that 21.33% of the patients had hypoglycaemia due to renal failure, 13.33% due to fasting and 10.67% due to taking antidiabetic drugs. But for 26.67% of cases, the causes were not specified [<xref ref-type="bibr" rid="scirp.93844-ref29">29</xref>] . Tumour causes including extrapancreatic could have been found, contributing to better management of hypoglycaemia. Further research into the exact cause of hypoglycaemia is necessary to avoid missing the diagnosis of a serious pathology. In the context of cancer, the hypoglycaemia should be suggestive of a paraneoplastic origin.</p><p>Indeed, the clinical manifestations of hypoglycaemia are of two types: neuroglycopenic and neurovegetative. The signs of neuroglycopenia correspond to a deficiency of glucose of the central nervous system and appear for a threshold of blood glucose lower than 0.50 g/l. They can result in confusion, behavioral problems, drowsiness, visual disturbances, transient motor deficiency, seizure and loss of consciousness. On the other hand, neurovegetative symptoms are related to stimulation of the autonomic nervous system by central hypothalamic activation, which is itself caused by hypoglycaemia, as soon as blood glucose falls below 0.55 g/l. Sweating, cravings and paresthesia are cholinergic signs, whereas anxiety, palpitation and tremor correspond to adrenergic manifestations [<xref ref-type="bibr" rid="scirp.93844-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref30">30</xref>] .</p><p>The presence of hypoglycaemia with collapse of insulinemia, peptide C and IGF-1, associated with an increase in IGF-2: IGF-1 ratio, leads to extrapancreatic tumour origin [<xref ref-type="bibr" rid="scirp.93844-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref21">21</xref>] . While an elevation of insulinemia, C-peptide leads to insulinoma [<xref ref-type="bibr" rid="scirp.93844-ref31">31</xref>] . In our case, these biological assessments were not available in our city. Blood samples must be taken to the capital for on-site examination or sent abroad. So the cost remains exorbitant for the majority of Malagasy people, who have no social cover or income sufficient to perform this kind of biological exam knowing that the average income of the Malagasy population is 348 USD per inhabitant per year according to a survey carried out in 2007 [<xref ref-type="bibr" rid="scirp.93844-ref32">32</xref>] . Thus, in our case, the diagnosis was directed to a paraneoplastic syndrome in view of the recurrent characteristics of hypoglycaemia in the absence of favourable factors, in particular the stopping of the oral antidiabetic, and the discovery of a gastric cancer.</p><p>Corticosteroid therapy, such as prednisolone at 2 mg/kg/day, is the basic treatment for paraneoplastic hypoglycaemia associated with tumour-specific therapy [<xref ref-type="bibr" rid="scirp.93844-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.93844-ref21">21</xref>] . In our case, the patient presented a recurrent hypoglycaemia because he refused chemotherapy and the corticotherapy was not conceivable because he had a gastrointestinal haemorrhage although this one is stopped after a well conducted treatment.</p></sec><sec id="s4"><title>4. Conclusion</title><p>In the context of cancers in diabetic patients, a paraneoplastic syndrome must be evoked in front of recurrent hypoglycaemia. It is still difficult to confirm in our country, given the lack of adequate technical platforms. A multidisciplinary collaboration between oncologists, endocrinologists and resuscitators would better support this entity.</p></sec><sec id="s5"><title>Conflicts of Interests</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s6"><title>Cite this paper</title><p>Randriamalala, R., Tika, L., Ranaivomanana, M., Rakotoniaina, A.I., Rafaramino, F. and Riel, A. (2019) Recurrent Hypoglycaemia in a Diabetic Patient Presented a Gastric Cancer: Think about Paraneoplastic Syndrome. Case Reports in Clinical Medicine, 8, 196-203. https://doi.org/10.4236/crcm.2019.87024</p></sec></body><back><ref-list><title>References</title><ref id="scirp.93844-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Cazabat, L. and Chanson, P. (2009) Hypoglycémie et insulinome. Annales D’endocrinologie, 70, S2-S11. https://doi.org/10.1016/S0003-4266(09)72470-9</mixed-citation></ref><ref id="scirp.93844-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Germain, C., Perrot, J.L., Labeille, B., Maitre, S., Gentil-Perret, A. and Cambazard, F. (2005) Uncarcinome hypoglycémiant. 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