Tuberous Sclerosis Complex with rare associated findings in the gastrointestinal system: a case report and review of the literature

Background Tuberous Sclerosis Complex (TSC) is a complex and heterogeneous genetic disease that has well-established clinical diagnostic criteria. These criteria do not include gastrointestinal tumors. Case presentation We report a 45-year-old patient with a clinical and molecular diagnosis of TSC and a family history of cancer, presenting two rare associated findings: gastrointestinal polyposis and pancreatic neuroendocrine tumor. This patient was subjected to a genetic test with 80 cancer predisposing genes. The genetic panel revealed the presence of a large pathogenic deletion in the TSC2 gene, covering exons 2 to 16 and including the initiation codon. No changes were identified in the colorectal cancer and colorectal polyposis genes. Discussion and conclusions We describe a case of TSC that presented tumors of the gastro intestinal tract that are commonly unrelated to the disease. The patient described here emphasizes the importance of considering polyposis of the gastrointestinal tract and low grade neuroendocrine tumor as part of the TSC syndromic phenotype.


Background
Tuberous Sclerosis Complex (TSC) is a genetic disorder with multiorgan involvement, a broad phenotype with inter and intra-familiar variability and well-established clinical diagnostic criteria (Table 1) [1][2][3][4]. The incidence of TSC is approximately 1 in 6000-10,000 live births, and in Europe its prevalence has been estimated to be 8.8/100,000 [5]. Germline pathogenic variants in TSC1 and TSC2 are identified in 75-90% of patients with the clinical diagnosis and at least 60% of TSC patients do not have a family history of the disease and are considered sporadic [6].
In this report, we describe a patient with the clinical and molecular diagnosis of TSC presenting with two rare associated findings: gastrointestinal polyposis and a pancreatic neuroendocrine tumor. A review of the literature on the subject is provided.

Case presentation
The patient, a 45-year-old male, was referred for genetic assessment due to clinical findings suggestive of Tuberous Sclerosis Complex (TSC) and polyposis of the gastrointestinal tract. Past medical history included symptoms such as significant seizures since infancy, mild cognitive impairment and adult-onset psychiatric symptoms. These symptoms prompted investigation with a brain magnetic resonance imaging (MRI), which showed subependymal nodules and cortical tubers, two major diagnostic criteria of TSC. Physical examination revealed facial angiofibroma but no additional cutaneous abnormalities were observed. Ophthalmologic, cardiac e pulmonary evaluations did not reveal presence of retinal hamartomas, cardiac rhabdomyomas or pulmonary lymphangioleiomyomatosis. Abdominal computed tomography (CT) scans showed an expansive lesion with heterogeneous enhancement, located in the lower pole of the right kidney, measuring 5.5 cm × 4.0 cm which was later confirmed as a renal angiomyolipoma, another classical sign of TSC. Multiple nodular lesions with arterial enhancement were identified in the liver, the largest one measuring 7.0 × 5.0 cm with features suggestive of secondary implants of unknown origin. In addition, abdominal imaging also showed an expansive lesion in the pancreatic body, with heterogenous enhancement, involving the splenic artery and measuring approximately 6.0 × 4.0 cm. In addition, the patient also had a long history of diarrhea and underwent colonoscopy and upper gastrointestinal endoscopy, revealing presence of more than 50 gastric, colonic and rectal polypoid formations (2 mm to 5 mm).
Family history of cancer was significant for presence of 2 relatives with central nervous system tumors (father and brother diagnosed at ages 62 and 57 years, respectively). Eight additional cancer unaffected siblings were reported. There was also no report of any other family member with clinical features of Tuberous Sclerosis Complex or other genetic conditions. Considering the clinical features of TSC and polyposis of the digestive tract, germline genetic testing was proposed with a next generation sequencing panel validated for large rearrangement screening including 80 cancer predisposition genes in a commercial la- Regarding pathology of the tumors, the haematoxylin and eosin stain (HE) performed in lesion of the right kidney revealed round cell renal tumor with typical morphology (Fig. 1a). The liver lesions were biopsied, showing a histologic pattern suggestive of a low-grade neuroendocrine tumor (NET) (Fig. 1c and e). Biopsies of the pancreatic lesion diagnosed a low-grade neuroendocrine pancreatic tumor (PanNET). Based on the major phenotypic criteria identified in the patient, the clinical diagnosis of TSC with a rare manifestation (PanNET) was established. Partial polypectomies were performed resecting three polyps from the gastric body, two polyps from the right colon and four polyps from the rectum. Histologic examinations of the gastric and colonic/rectal polyps revealed fundic gland polyps and tubular adenomas with low-grade dysplasia, respectively (Fig. 2). Immunohistochemistry (IHC) was performed in the biopsy of the right kidney lesion and demonstrated positive expression of melanoma antigen (Melan A) (Fig. 1b), melanosomal glycoprotein gp100 antigen (HMB45) and smooth muscle actin antigen. The lesions in the liver were confirmed by IHC, showing positivity for multiple citokeratins antigens (40,48, 50 e 50,6 kDa), chromogranin A antigen (CGA) (Fig. 1d), and synaptophysin (Sinapto) (Fig. 1f).

Discussion and conclusions
TSC is an autosomal dominant disease associated with cancer predisposition and multisystemic involvement mainly due to hyperactivation of the mTOR pathway, secondary to loss of function mutations in TSC1 and TSC2 [7]. Approximately 15% of the pathogenic variants identified in TSC2 and 8% of those identified in TSC1 are large gene rearrangements (LGR) [8], and therefore, genotyping using a methodology that allows LGR detection is important in a diagnostic workup. Although criteria for clinical diagnosis of TSC are well established, expressivity is highly variable, even within families with multiple carriers of the same pathogenic variant and simplex cases with de novo mutations are not uncommon reaching up to 86% in some cohorts [9]. The recent, increased access to multigene panel testing to investigate suspected hereditary cancer has resulted in molecular diagnosis of individuals without the classic clinical criteria or apparently "sporadic" tumors or isolated clinical features of the disease.
In this report, we describe a patient fulfilling criteria for the clinical diagnosis of TSC, such as cortical tubers, facial angiofibroma and renal angiomyolipoma (Table 1 and Fig. 1a and b) carrying a previously described large TSC2 rearrangement with two uncommon clinical manifestations of the disease: gastrointestinal adenomatous polyposis and a metastatic pancreatic neuroendocrine tumor. The occurrence of numerous colonic and rectal polyps, characterized in this patient as tubular adenomas, is a symptom associated with gastrointestinal polyposis and colorectal cancer syndromes, such as Familial adenomatous polyposis (FAP), a rare autosomal, dominant hereditary disease [10]. FAP is caused by a germline mutation in the APC gene [11]. Besides FAP, other syndromes could be associated, including mismatch repair deficiency (biallelic MLH1, MSH2, MSH6, PMS2 gene mutations), polymerase proofreadingassociated polyposis (POLD1, POLE genes), juvenile polyposis (SMAD4, BMPR1A genes) and MUTYH-associated polyposis [12]. Sequence changes and exonic deletions/duplications were evaluated in all of these associated genes and negative results exclude these syndromes in this patient.
The heterozygous TSC2 exon 2-16 deletion identified is also known as deletion of exons 1-15 in the literature. Truncating variants including gross deletions in TSC2 are known to be pathogenic. The 5′ end of the deletion remained undetermined as it was beyond the assayed region and the 3′ boundary was probably within intron 16 of the TSC2 gene. This deletion is expected to result in complete removal of the TSC1 binding domain (T1BD) the N-terminus of the TSC2 protein in one of the alleles. This domain is critical for TSC1-TSC2 interaction (formation of TSC complex) and abnormal or absent TSC complex results in TSC2 ubiquitination and degradation. This in turn eliminates inhibition of the conversion of Rheb-GTP which accumulates and directly activates the mTORC1 pathway [13,14].
Three previous reports describe TSC patients carrying the same germline TSC2 exon 2-16 (a.k.a. exon 1-15) deletion [15][16][17]. However, according to the information available, none of them presented the uncommon clinical features reported here (neuroendocrine tumors or gastrointestinal polyps) (Tables 2 and 3); although it is possible that due to their ages, these phenotypes would not yet be identifiable. Interestingly, Mortaji et al., 2018 described an adult TSC patient who presented both, a pancreatic NET and gastrointestinal (GI) polyps. But different from the case presented here, they were hamartomatous/inflammatory polyps [40]. Although rectal polyps are included as a minor clinical diagnostic criterion for TSC, there is no mention to polyps in other portions of the GI tract and the vast majority of polyps described in TSC patients are hamartomatous [19,43]. Gastric fundic polyps (FGPs) are considered hamartomas and tuberin protein (codified by TSC2 gene) seems to play an important role in pathogenesis of sporadic FGPs by deregulation of cell proliferation. The altered cellular localization of tuberin interrupts its interaction with hamartin protein (codified by TSC1) preventing the formation of TSC complex that regulates mTORC1 pathway, responsible for cell proliferation and protein synthesis signaling pathways. In addition, altered cellular localization of tuberin may preclude its negative regulation of gene transcription mediated by tuberinassociated proteins glucocorticoid receptor (GCR) [44]. We identified only one case report of an adolescent TSC patient with tubular adenomatous polyps of the GI tract. The report by Digoy et al. (2000), and the case reported here, presented with a high number of GI tract polyps (unlikely somatic in origin) and a negative comprehensive evaluation of known polyposis genes, reinforce that GI polyposis with different histologies is likely part of the TSC phenotype and should be considered in the differential diagnosis [18]. Of note, glandular fundic polyps and tubular adenomatous polyps could be two different expressions of the same germline variation.
Finally, pancreatic neuroendocrine tumors (PanNET) are most commonly sporadic but have been reported previously in association with TSC and in other inherited cancer syndromes such as von Hippel-Lindau Case report: 12 yo male with a GH-oma and acromegalic gigantismo. NA [22] Case report: 25 yo female with hyperprolactinaemia, amenorrhoea and galactorrhoea after delivery of 3rd child. NA [23] Case report: 32 yo male with an ACTH-oma and Cushingoid features. NA [24] Case report: 13.5 yo male with an ACTH-oma, short stature, abnormal distribution of fat tissue and rounded face, plethora and acne.

NA
Parathyroid NET [25] Case report: 20 yo female with parathyroid hyperplasia, and on autopsy multiple endocrine adenomatosis affecting, in addition to the parathyroid, the pituitary (a non-functioning pituitary adenoma), adrenals and pancreas (islet cell tumour).

TSC2
Pancreatic NET [29] Case report: 24 yo female with insulinoma and symptomatic hypoglycaemia and novel onset of seizures NA [30] Case report: 23 yo male with insulinoma and recurrent seizures presented after 15 years of being seizure free NA [31] Case report: 34 yo male with a pancreatic gastrinoma, presenting with reflux esophagitis and massive weight loss NA [32] Case report: 28 yo male with insulinoma and behavioral changes characterised by episodes of agitation and, at other times, lethargy NA [33] Case report: 18 yo female with insulinoma with symptomatic hypoglycaemia. NA [34] Case report: 12 yo male with a malignant islet cell tumour TSC2 (nonsense) [35] Case report: 43 yo male with insulinoma and episodes of Episodes of sweating and dizziness. NA [36] Case report: 6 yo male with a malignant islet cell tumour of pancreas TSC2 (nonsense) [37] Case report: 39 yo male with a pancreatic islet cell tumor and lichenified hyperpigmented plagues (paraneoplastic process) TSC2 (1 bp ins) [38] Case report: 31 yo male with TSC, multiple congenital subependymal nodules, bilateral cortical tubers, seizures and a malignant (metastatic) pancreatic neuroendocrine tumor.
NA [39] Description of 5 patients with TSC (clinical diagnosis) and pancreatic tumors, 2 of them confirmed pancreatic neuroendocrine tumors, localized in the pancreatic tail (5 yo male with a 26 mm lesion and 12 yo male with a 10 mm lesion).
NA [40] Case report: 35 yo female with TSC, adenoma sebaceum, shagreen patch and hypopigmented macules, bilateral renal angiomyolipomas and Hurthle cell adenoma. Multiple benign hamartomatous and inflammatory-type polyps in the cecum, sigmoid colon, and rectum. Pancreatic well-differentiated neuroendocrine tumor.  (Table 3). In a previous report describing molecular features of TSC patients, none of the probands reported GI tract polyposis [49].
In conclusion, there is currently no recommendation for GI polyp or PanNET screening, probably given the rarity of these findings, in TSC patients. Gastric and colorectal polyps and PanNETs are also not considered as phenotypic criteria for the clinical diagnosis of the syndrome. The patient described here, with confirmed molecular diagnosis of TSC underscores the importance of considering GI tract polyposis and NETs as part of the syndromic phenotype.