Duodenogastric Intussusception in a 14-Week-Old Infant with Donohue Syndrome: Case Study

Donohue syndrome (DS) is a rare recessively inherited disorder characterized by severe insulin resistance caused by genetic defects affecting the insulin receptor. The classical clinical characteristics include severe intrauterine growth restriction, craniofacial dysmorphic features, body and skin features, and soft tissue overgrowth. Postnatal growth retardation, cardiac, gastrointestinal, and renal complications, and infection susceptibility develop within the first few months of life, leading to a short life expectancy (<2 years). The classical metabolic abnormalities vary from fasting hypoglycemia to postprandial hyperglycemia with severe hyperinsulinemia. We present the case of a 14-week-old infant with DS who developed cardiac, renal, hepatic, pancreatic, and gastrointestinal features, all of them previously reported in infants with DS. The gastrointestinal features started during the first week of life and included abdominal distension, feeding difficulties, intermittent vomiting, and two episodes of intestinal obstruction. The diagnosis of duodenogastric intussusception was made, and this previously unreported complication tragically resulted in mortality. We discuss how basic mechanisms of cross-talk between insulin and insulin-growth factor 1 receptors could be linked to hyperinsulinemia and its associated comorbidities.


Introduction
Donohue syndrome (DS) is the most severe manifestation of insulin resistance (IR) and is caused by homozygous or compound heterozygous mutations in the insulin receptor (INSR) gene.
Te neonatal clinical phenotype includes intrauterine growth restriction (IUGR), morphological aberrations, fasting hypoglycemia, postprandial hyperglycemia, hyperinsulinemia, and initial resistance to ketosis [1].Postnatal growth retardation, cardiac, gastrointestinal, and renal complications, and infection susceptibility develop within the frst few months of life.
Ovarian enlargement and juvenile granulosa cell tumors may be associated.
Te prognosis is poor, with cardiac, gastrointestinal, and infectious morbidity and high mortality during the frst years of life.
Te main biochemical features are defned by abnormal glucose homeostasis, with hypoglycemia, postprandial hyperglycemia, and severe hyperinsulinemia, and are present soon after birth.
Te most common pharmacological approach for overcoming tissue insulin resistance is the use of recombinant human insulin-like growth factor 1 (IGF 1 ), although the complexity of its various tissue efects remains only partially understood.
We report the case of a 14-week-old infant with DS and rapid development of classical cardiac, renal, hepatic, and pancreatic complications.Te gastrointestinal involvement presented initially as feeding difculties, intermittent vomiting, and abdominal distension without organomegaly and worsened rapidly, culminating in a fatal duodenogastric intussusception, confrmed by radiological and histopathology studies.
With this report, we would like to raise awareness of the possibility of early severe gastrointestinal dysmotility in infants with DS.

Case Report
We describe the case of a male newborn, ffth child of a consanguineous Caucasian couple (frst cousins), born at 31 weeks of gestation, weighing 950 g (<<−3 SD), and measuring 43 cm (−1 SD).
Severe intrauterine growth retardation was evident throughout pregnancy, and at birth, the newborn appeared markedly emaciated, with no subcutaneous fat, muscular hypotrophy, and dysmorphic features: elfn face, low-set ears, broad nasal tip, thick lips with broad mouth, macroglossia, generalized hypertrichosis, small thorax, distended abdomen without hepatosplenomegaly, and macrogenitosomia.Acanthosis nigricans was absent.
On the frst day of life, the infant had hyperglycemia (12 mmol/L) with very high random insulin (932 mUI/L) and C peptide (3.46 nmol/L) levels.Complementary endocrine fndings included low levels of insulin growth factor 1 (IGF 1 ) (12 µg/L) and insulin growth factor-binding protein 3 (IGFBP 3 ) (0.35 mg/L) with a normal growth hormone level (26 mU/L) and an undetectable leptin level (<1 ng/mL).Echocardiography indicated a 3 mm ductus arteriosus with no other morphological abnormalities.
Te constellation of intrauterine growth restriction, distinctive clinical features, and disrupted glucose homeostasis strongly suggested the diagnosis of Donohue syndrome (DS).
Te patient's parents provided informed consent for molecular genetic analysis, which confrmed the diagnosis of DS through the detection of the homozygous variant c.1106T > A in exon 4 of the insulin receptor gene.Tis variant results in an amino acid substitution of Ile369 with Asn (I369N) within the insulin-binding domain.Both parents were heterozygous carriers of this missense variant, which was not previously reported.
To manage the disrupted glucose homeostasis, continuous subcutaneous administration of recombinant human IGF 1 (rhIGF 1 ) was initiated at 15 days of life with a progressively adjusted dosage from 60 to 500 µg/kg/day, resulting in improved glycemic control (glucose level between 4 and 10 mmol/L) without hypoglycemia, normalized IGF 1 and IFGBP 3 , and unchanged insulin levels.
Te echocardiography follow-up revealed severe left ventricular hypertrophy at the age of 14 days and global myocardial hypertrophy at 11 weeks of age, with interventricular septal thickness at diastole of 8 mm, left ventricular outfow tract obstruction, and ventricular ejection fraction at 37%.Treatment with a β-blocker (propranolol) was proposed, but not immediately initiated.
At the age of 10 days, the neonate developed blood emesis with exacerbation of the abdominal distension, without hepatomegaly.Te hepatic profle revealed elevated transaminase levels, prolonged prothrombin time, low serum albumin concentrations, and elevated total and conjugated bilirubin levels.Pancreatic exocrine dysfunction was suspected based on lipase levels and fecal elastase levels, although a confrmatory examination was not conducted (Table 1).
Te baby was initially fed by parenteral and then enteral nutrition (by nasogastric tube), with an adequate caloric intake (130 kcal/kg/d) and low weight progression.
At 11 weeks of age, the infant had a new episode of acute abdominal distension with vomiting.Radiological evaluation revealed signifcant gastric distension on plain flm radiography and duodenogastric intussusception on ultrasonography (Figure 1).Upper endoscopy confrmed the duodenogastric intussusception (Figure 2) and revealed a hypertrophic, pale, and edematous gastric mucosa with enlarged folds.Attempt to reduce intussusception by endoscopy was unsuccessful.Histological examination revealed an unremarkable duodenal mucosa with difuse thickening of the antral gastric mucosa, crypt hypertrophy, and lymphoplasmacytic infltration.Immunohistochemical analysis was negative for Helicobacter pylori and Cytomegalovirus infections.
To overcome the partial gastric outlet obstruction and optimize the enteral feeding, gastrostomy and gastrojejunal tubes were placed, but there was little or no clinical improvement.Surgery was discussed, but due to fragile cardiac condition of the infant, temporizing surgical management was considered.
Te infant's clinical evolution did not improve, and he required increasing supplemental oxygen and developed more frequent episodes of tachyarrhythmia and hypertension.Continuous positive airway pressure support was provided.
At the age of 14 weeks, the infant's clinical status deteriorated, with severe abdominal distension and incoercible vomiting, suggestive of new episode of intestinal intussusception with associated cardiopulmonary distress, ultimately leading to death.Autopsy was not performed (parental decision).

Discussion
Our patient presented with common clinical and biological features of DS.Facial, skin, and bodily features, overgrowth of soft tissues, and organ dysfunction (renal, hepatic, pancreatic, and gastrointestinal) were present at birth or developed early during the neonatal period.His initial biological picture was also classic, with severe hyperinsulinemia, postprandial hyperglycemia, and low growth hormone level.
We hypothesized that the variant c.1106T > A in exon 4 of the insulin receptor gene, found in our patient and his 2 Case Reports in Pediatrics

Multiorgan impairment
Second episode of intestinal obstruction with cardio-respiratory distress and death Glycemia 5 IGF 1 � insulin-like growth factor 1, IGFBP parents, likely alters insulin-binding kinetics, although this has not yet been demonstrated.Several analytical criteria support the pathogenic nature of this variant, including its absence in the general population (gnomAD) and bioinformatics prediction indicating potential pathogenicity.
Gastrointestinal picture of DS includes intrauterine growth restriction, poor postnatal weight gain, and abdominal distension.Recently, additional digestive manifestations, such as intrinsic gastrointestinal dysmotility, hepatic dysfunction, and pancreatic exocrine insufciency, were reported [8].
Our patient's gastrointestinal features and evolution, including early feeding difculties, repeated vomiting of unclear cause, and progressive to permanent abdominal distension with 2 episodes of exacerbation (acutely distended abdomen with massive vomiting), culminated in the diagnosis of duodenogastric intussusception (ultrasound and endoscopic diagnosis).Tis entity was not previously reported in patients with DS, and its clinical, radiological, and histological characteristics, as found in our patient, could add important insights into the complex gastrointestinal picture of DS.Ultrasonography remains a valuable imaging study option for gastrointestinal emergency diagnosis in infants [9,10].
Te severity of this gastrointestinal complication in the context of rapid progressive hypertrophic cardiomyopathy with associated compromised hemodynamic stability contributed to fatal evolution of our patient.
DS is an extremely rare form of insulin resistance in the pediatric population, and the main pathophysiological mechanism of this glucose homeostasis abnormality is a result of genetic defects in the INSR.
Insulin and IGF 1 act via structurally and functionally similar tyrosine kinase receptors and have similar physiological efects on vital metabolic activities and developmental processes (cellular growth, proliferation, diferentiation, apoptosis, and survival) [11,12].Receptors' structural and functional homology may become signifcant only at supraphysiological concentrations of insulin and IGF 1 .
Te molecular anomalies of the INSR, the insulin mimetic on the IGF 1 receptors (IGF 1 R) leading to their pathological hyperactivation, and IGF 1 R tissue expression contribute to the phenotypic and biological aberrations in DS.
IGF 1 R is lowly expressed in insulin-responsive tissues, such as adipocytes [13], which contributes to reduced subcutaneous fat in DS.
IGF 1 R is expressed in the cardiac tissue, and hyperinsulinemia-mediated IGF 1 R signaling is implicated in cardiomyocyte hypertrophy [14].
IGF 1 is involved in the tubular handling of sodium, water, calcium, and phosphate and regulates tubular gluconeogenesis [3].Insulin signaling through the IGF 1 R may contribute to renal enlargement and electrolyte imbalance observed in patients with DS.
Te insulin/IGF 1 system is vital for mammalian sexual development and reproduction [15].In DS, the overactivation of this system results in genital enlargement and biochemical abnormalities (elevated estradiol and testosterone levels).Activation of the IGF 1 R by insulin, along with low circulating growth hormone levels, may serve as a protective mechanism against ketoacidosis in patients with DS [1].
Te gastrointestinal tract is the primary target of IGF 1 action, which stimulates the proliferation of intestinal epithelial and muscle cells [16].In mice, IGF 1 overexpression has been shown to lead to a normal gastrointestinal epithelium, but an expanded submucosa with hyperplastic and hypertrophic muscularis propria [17].
Did our patient's tragic evolution (duodenogastric mucosal intussusception in the context of severe myocardial hypertrophy) refect the natural progression of DS or was related to rhIGF 1 treatment?rhIGF 1 therapy appears to improve glycemic control in most patients with DS, although there are theoretical concerns that rhIGF 1 may worsen DS complications.Clinical data on the pharmacological efects of rhIGF 1 (benefcial or deleterious) on hypertrophic cardiomyopathy development and progression in DS patients are limited.Additionally, abdominal distension was present in almost all reported DS cases, and the infants not treated with rhIGF 1 died [18,19].Possible mechanisms involve IGF 1 and insulin signal transduction inhibiting apoptosis and stimulating cellular proliferation and carcinogenesis [20].

Conclusion
Our observation sheds light on the complex phenotypic features of DS patients, with particular attention to the gastrointestinal manifestations.Although less prevalent and less diagnosed, they display signifcant variability in clinical presentation and severity and infuence the patient survival.Accumulating clinical evidence may eventually lead to earlier diagnosis of DS gastrointestinal dysfunction and timely and appropriate intervention.

Figure 1 :
Figure 1: Longitudinal and transverse ultrasound views of the pylorus displaying intussusception.

Table 1 :
Patient's clinical and biochemical evolution.