Current status of the diagnosis and treatment of gastrointestinal schwannoma

Abstract

Gastrointestinal schwannoma is a rare, slow-growing and benign tumor that mostly originates in the Auerbach myenteric nerve plexus in the gastrointestinal tract. The clinical manifestations may be associated with the location, size, differentiation type, and degree of malignancy of the tumor. Endoscopy, ultrasound and imaging examinations serve an important auxiliary role in the clinical identification, diagnosis and differential diagnosis of lesions; assessment of risk; and preparation for surgery. S-100 positivity is a hallmark of schwannoma. CD34, CD117, discovered on GIST-1, P53, ALK, β-catenin, smooth muscle actin and Desmin negativity are helpful for the identification of other gastrointestinal stromal tumors. Surgical removal of the tumor is the main treatment for schwannoma. Benign gastrointestinal schwannoma has a good prognosis without recurrence and metastasis; malignant transformation is extremely rare and has a poor prognosis.

1. Introduction

Schwannomas are caused by the excessive proliferation of Schwann cells in nerve sheaths. They grow slowly and can occur in any part of the body, such as the limbs, head, spinal cord and peripheral nerves of the central nervous system, but are rarely seen in the gastrointestinal tract (1). Gastrointestinal schwannoma (GIS) was first reported by Daimaru in 1988 (2), and it is being diagnosed more frequently with recent advances in diagnostic technology and immunohistochemistry. Schwannomas account for 2–6% of gastrointestinal mesenchymal tumors (3,4); 60–70% occur in the stomach, followed by the colon and rectum (3%), and their occurrence in the esophagus and small intestine is even rare (5). They are classified as mesenchymal or neuroectodermal tumors, and this type of tumor originates in the gastrointestinal wall and includes gastrointestinal schwannoma (GIS), gastrointestinal stromal tumor (GIST), leiomyoma, leiomyosarcoma, neurofibroma, lipoma, ganglioneuroma, paraganglioma, granulosa cell tumor and globular tumor. GIS originates from the Auerbach myenteric plexus in the gastrointestinal nerve plexus (2). The most common clinical feature is submucosal lesions, which are usually found accidentally during gastrointestinal endoscopy, endoscopic ultrasonography, imaging or abdominal surgery. However, so far, due to its low incidence, malignant transformation occurs in only 2% of cases (6), it has not been studied comprehensively enough, and most reports on GIS are case reports. The diagnostic accuracy is diminished by the morphological diversity of GIS, and it is difficult to develop a unified diagnostic standard (7–12). The clinical manifestations, commonly used laboratory examinations, pathological features, differential diagnosis, treatment and prognosis were reviewed, aiming to provide a reference for GIS diagnosis and treatment.

2. Pathogenesis

Molecular mechanism

The pathogenesis of schwannomas is not yet fully understood. Studies have been limited to classic soft tissue schwannomas (such as vestibular nerves and trigeminal schwannomas), which are mostly associated with genetic diseases, such as neurofibromatosis type 2 (NF2) defects, and involve the process of chronic peripheral nerve injury and over-repair (13–15). When peripheral nerves are damaged, Schwann cells in a static state are activated to initiate a redifferentiation program for repair; however, if the NF2 gene is abnormal, large numbers of Schwann cells will proliferate due to the disruption of redifferentiation, which will eventually lead to tumor formation (16). Lasota et al (17) found that NF2 in GIS exhibited the loss of heterozygosity, and inactivating mutations were identified in only 1 of 20 analyzed tumors.

Gastrointestinal malignant schwannoma (GIMS) may be associated with neurofibromatosis type 1 (NF1). In the study of NF1, it has been shown that NF1 gene mutations and/or the loss of heterozygosity may exist in 50% of GIS (17), resulting in the loss of neurofibrin (encoded by NF1), thereby accelerating the inactivation of Ras GTP and leading to increased RAS expression. The interaction between the loss of neurofibrin and the increase in RAS expression leads to the enhancement of mitotic signals and dysregulation of cell cycle growth regulation, promoting tumor malignancy (18).

3. Clinical features

The age of GIS occurrence is mostly between 50 and 80 years (5). Some studies have reported that GIS occurrence has a female preponderance (2,6,10). GIS is occasionally seen in gastrointestinal endoscopy and imaging examinations; these tumors are mostly benign with relatively slow growth, which causes nonobvious gastrointestinal symptoms in most patients. The corresponding symptoms depend on the tumor location, size, differentiation, and degree of malignancy.

When the tumor occurs in the stomach, it often causes upper abdominal discomfort, including atypical abdominal pain, fullness, nausea, acid reflux, vomiting and anorexia; if the tumor develops in a certain location, such as the cardia and pylorus, as the tumor expands, it can cause eating obstruction, nausea and vomiting. In the intestine, the tumor can cause obstruction, intussusception and melena, as the tumor grows through the mucosa and forms an ulcer. The excessive growth of GIS may involve other organs and cause corresponding symptoms, such as large gastric schwannoma that causes atypical chest pain (19), pleural effusion (20) and other unique symptoms. In general, a tumor size in the gastrointestinal tract over 5 cm is known to have a high risk of possible complications and thus needs curative resection; if not resected, the propensity to become malignant is high.

When tumor growth causes compression or ischemic necrosis, acute symptoms, such as abdominal pain, obstruction, bleeding, perforation and other clinical manifestations, may appear. Some cases have also reported schwannoma causing intussusception (21). In addition, as a benign tumor, it can also cause symptoms associated with malignant tumors. Case reports have also found that GISs can cause Lambert-Eaton myasthenia-like syndrome (22) and other paraneoplastic syndromes; other symptoms can also include secondary membranous nephropathy (23), proteinuria and lower extremity edema.

At present, there are few reports on GIMS, and their symptoms can be similar to those of benign tumors, but malignant behaviors such as metastasis and cachexia may also occur (24–27).

4. Common auxiliary examinations and characteristics

Digestive tract (ultrasound) endoscopy, abdominal ultrasound, computed tomography (CT), magnetic resonance imaging (MRI), ¹⁸fluorodeoxyglucose positron emission tomography (¹⁸FDG-PET) and other examinations are routine examinations for gastrointestinal diseases. For GIS that resembles as other common tumors of the bowel, the aforementioned examinations are nonspecific, not pathognomonic, and only provide a reference for diagnosis (28,29).

Endoscopy and ultrasound endoscopy

Gastrointestinal endoscopy is one of the most common examinations of the digestive tract. It can clarify the location, size, and mucosal changes of GIS; however, considering that GIS mostly occurs in the muscularis propria or submucosa, it mostly appears as protruding lesions under endoscopy, so patients are mostly treated for GIST. Conventional endoscopic tissue biopsy usually only shows chronic inflammatory manifestations of the mucosa, so it is difficult to diagnose tumors. Twenty-five to 50% of tumors will cause ulcers in the central area as the volume increases, leading to ischemic changes in the surrounding mucosa (30). Similarly, GIMS also involves bleeding from malignant ulcers, so bleeding, necrosis, and ulcer changes can provide help in identifying benign and malignant tumors.

Endoscopic ultrasound-guided biopsy is currently an important examination for the preoperative diagnosis of gastrointestinal tumors, especially submucosal tumors, and increases the chances of preoperative diagnosis by 10% (31,32). It generally includes endoscopic ultrasound-guided fine-needle aspiration and trucut biopsy (EUS-FNA and EUS-TCB), but there are significant differences in the number of tissue samples obtained due to differences in puncture techniques, so the specificity of EUS-FNA and EUS-TCB is low (52 vs. 55%) (33). The latest research found that using EUS-FNA-derived RNA for mutation analysis is highly feasible and provides reliable results (34); therefore, for submucosal GIS, ultrasound-guided biopsy is recommended as a routine examination method to confirm the preoperative diagnosis.

Ultrasound examination

Abdominal ultrasound examination is currently widely used to locate abdominal masses and evaluate blood flow conditions. Contrast-enhanced ultrasound is a non-invasive inspection method that does not use radiation to examine the perfusion status of the lesion. Because it can examine the blood perfusion of a tumor, it is very useful in the differential diagnosis of lesions (35). Under ultrasound, GIS mostly appear as hypoechoic masses with clear boundaries and insufficient internal blood flow. When contrast-enhancing agents are used for enhanced dynamic imaging, gastric schwannoma exhibits a rapidly progressing washout phenomenon, while on static images, the tumor appears with moderate echo enhancement (36).

Abdominal computed tomography (CT) and magnetic resonance imaging (MRI)

GISs can occur in any part of the gastrointestinal tract, and most of them grow contralaterally to the mesenteric attachment (37). Under CT, it mostly appears round, with uniform density or density lower than soft tissue and clear boundaries. A homogeneous pattern of tumor attenuation is the most consistent feature of GIS on CT scans. However, there are also a small number of cases with slow and progressive enhancement, suggesting that the enhancement of gastrointestinal schwannomas occurs over time, with peak enhancement occurring during the equilibrium phase (38). The most striking difference in the CT features of GIS compared with those of GIST is the rare presence of hemorrhage, necrosis and cystic changes. It shows fewer signs of abdominal parenchymal organs, lymph node malignant metastasis and abdominal effusion, which is helpful for the differentiation of benign and malignant tumors. Compared with CT examination, MRI is superior to CT in distinguishing GIS and GIST. On T1-weighted images, tumors often show lower signal intensity, while on T2-weighted images, they often show higher signal intensity (39).

¹⁸FDG-PET

FDG-PET is mainly used to assess the malignant potential of tumors and the recurrence and metastasis of malignant tumors. It is one of the important preoperative methods for distinguishing benign and malignant lesions from atypical gastrointestinal tumors. A previous report demonstrated that benign GIS showed increased FDG intake and large metabolic changes, which contrasted with the low metabolic changes of benign tumors on FDG-PET (40). Miyake et al (41) proposed that this observation may be associated with the lymphatic sheath around the tumor, but there is no relevant experimental evidence. Therefore, the role of FDG-PET in the assessment of benign and GIMS and their differentiation from other interstitial tumors needs further study. FDG-PET may be of limited value as a preoperative diagnostic technique for the assessment of GIS.

Hematological examinations

When tumors cause hemorrhage, decreases in hemoglobin and albumin levels might occur in patients with GIS. Reports have shown that common serum tumor markers, such as fetoprotein, CEA and carcinoembryonic antigen, were within the normal range (42,43), but occasionally increased CA19-9 was observed (44). Notably, Shu et al (45) pointed out that one patient had elevated serum neuron-specific enolase (NSE) levels. NSE is an acid protease that is specific to neurons and neuroendocrine cells, and is highly concentrated in nerve cells, neuroendocrine cells and tumor cells (45). Therefore, it is feasible that the immunohistochemistry of GIS would show a positive NSE result.

5. Pathological characteristics

General features

GIS mostly exhibits exogenous or intraluminal bulging growth, with sizes between <1–28 cm (3,5); most of them occur as single tumors, and multiple tumors are rare (46). The solid mass is round or oval to the naked eye, with clear boundaries, a gray or yellowish-white cut surface, no intact surrounding capsule, and necrosis, hemorrhage, calcification, and cystic changes in the central area are rare.

Cytological characteristics

Classic soft tissue schwannomas have two alternating structures. Antoni A is a dense growth of spindle cells arranged in a fence-like structure to form Verocay bodies with abundant blood vessels, and Antoni B is characterized by a loose distribution of spindle cells with round or slender nuclei, containing a large amount of myxoid stroma and xanthomatous histiocytes (47). However, Bohlok et al (6) found that only 12.5% of cells have two structures in the GIS, with only a structure similar to Anotoni A lacking Verocay bodies. Microscopically, the short spindle cells in GIS are arranged in a palisade shape with unclear borders, their cytoplasm is slightly eosinophilic, and their nucleus is deep and round or oval. The most significant feature of GIS is the short spindle cell in the center of the tumor and the chronic inflammatory cell infiltration around the tumor, forming a prominent lymphoid cuff, which can aid in distinguishing GIS from other mesenchymal tumors. Nuclear atypia with hyperchromasia is common, and the mitotic count rarely exceeds 5/50 high-powered field, which can be used as a standard for the classification of benign and malignant tumors (6,47,48).

Immunohistochemistry

Immunohistochemical examination is the gold standard for diagnosing GIS. S-100 is a group of highly acidic calcium-binding proteins that are widely distributed in neural crest cells and their tumors. Because the Antoni A-like area in GIS can show the diffuse and strong expression of S-100, the strong positivity of S-100 makes it a specific marker, with an expression rate of 97.9% (6). In addition, CD34 and Vimentin are occasionally positive, and other immunological markers, NSE, CD34, CD117, discovered on GIST-1 (DOG-1), P53, ALK, β-catenin, smooth muscle antigen (SMA) and Desmin negativity, provide the main evidence for differential diagnosis (46). In addition, GIS derived from non-Schwann cells may be positive for specific markers, such as melanin, which is indicative of melanoma schwannoma. For GIMS, the degree of invasion is mostly associated with the Ki-67 index. It is generally believed that Ki-67 >5% is considered to be malignant, and >10% is considered to be malignant (3,5). However, Ki-67 alone is not enough to judge the degree of tumor malignancy. It is also necessary to consider factors such as the tumor size, mitotic index, MIB-1, tumor recurrence, and local or distant metastasis (49–52).

GIMS is positive for glial fibrillary acidic protein, vimentin, NSE and CD68, and negative for S-100, CD117, CD 99, CD34, CD20, desmin and SMA (53).

Malignant schwannomas mostly contain dedifferentiated Schwann cells, and the synthesis of s-100 is decreased, so the expression of s-100 will decrease as the malignancy of schwannomas increases (54).

6. Differential diagnosis

GIS is a type of gastrointestinal mesenchymal tumor. Due to its low incidence, the clinical misdiagnosis rate is up to 96.7% (55). The immunohistochemistry features of GIS, GISTs and other tumors are described in Table I.

Table I.

Differential diagnosis of GIS by immunohistochemistry.

	GIS	GIMS	GIST	Neurofibromas	Melanoma	Leiomyomas	Leiomyosarcoma
S-100	+++	+↓	–	+/++	++	–	–
Vimentin	+++	+	–	+/++	++	++	++
NSE	++	+	–	++	–	–	–
Desmin	–					+++	+++
CD34	–		++	++	–	–	++
CD117(c-KIT)	–	–	++		±	–	–
DOG-1	–		+++				–
CD56	+++		–	–		–	–
CD68	+++			–
GFAP	+	+	–	–		–
SMA	–	±a				+++	+++
HMB-45					+++
LCA		–			–
PCNA						+	+++

↓, Expression decreases as the degree of malignancy increases.

^aNegative (26) or positive (27) are reported. GIS, gastrointestinal schwannoma; GIMS, gastrointestinal malignant schwannoma; GIST, gastrointestinal stromal tumor; NSE, neuron-specific enolase; DOG-1, discovered on GIST-1; GFAP, glial fibrillary acidic protein; SMA, smooth muscle antigen; HMB-45, human melanoma black45; LCA, leucocyte common antigen; PCNA, proliferating cell nuclear antigen.

GIST

Due to the prevalence, clinical symptoms, morphology and growth patterns of GIST being very similar to those of GIS, GIS is most commonly misdiagnosed as GIST, and 10–30% of GIST becomes malignant (56). Therefore, the ability to correctly identify the nature of the tumor plays a key role in further treatment and prognosis. Preoperative imaging and endoscopy can provide limited help, but if GIS is not accurately diagnosed, clinicians usually treat it as GIST. Generally, GIST tumors have a cut surface that is gray or gray-red, rich blood supply, necrosis, liquefaction, calcification, and are commonly cystic, and the behavior is very different from that of GIS. Microscopically, it is composed of spindle cells with diverse morphological arrangements and no palisade shape. CT shows obvious enhancement, and the immunohistochemical phenotype is CD117, CD34 and DOG-1 positivity, and S-100 negativity, which is the most important distinction from schwannoma.

Gastrointestinal smooth muscle tumor

It rarely occurs in the colon and very rarely in the small intestine. The CT findings are often uneven and obviously enhanced. The interior of leiomyoma is gray, solid, fibrous and tough. The cut surface of the leiomyoma can be gray-red and resemble fish flesh, accompanied by hemorrhagic necrosis and cystic degeneration. Microscopically, the spindle cells appear weaved or bundled, and leiomyosarcoma cells have obvious atypia, accompanied by obvious necrosis and mitosis. No muscle-derived markers are positive, and S-100 is negative or weakly positive.

Gastrointestinal lymphoma

Due to the lymphocyte cuff of GISs, they are easily misdiagnosed as gastrointestinal lymphoma during preoperative needle biopsy (57), and CT findings of gastrointestinal lymphoma are similar to those of GIS, so it is not uncommon to misdiagnose GISs as lymphoma. Gastrointestinal lymphoma is usually accompanied by extensive mesenteric or retroperitoneal lymphadenopathy, whose features can be distinguished from GIS. Additionally, gastrointestinal lymphomas are commonly accompanied by adenopathy in the supporting mesenteries and retroperitoneum, so adenopathy is a helpful distinguishing feature for lymphoma (58).

Malignant tumors of the gastrointestinal tract

These tumors grow aggressively and are not clearly demarcated from the normal gastrointestinal wall. They are characterized by a stiff tubular wall, narrow lumen, early gastrointestinal obstruction and local lymphadenopathy. The GIS boundary is clear, lymph nodes are rarely enlarged, and digestive tract obstruction appears late. Since gastrointestinal cancer mostly originate in the mucosal layer, the nature of gastrointestinal malignant tumors can be determined by endoscopic biopsy pathological examination, gastrointestinal cancer can be diagnosed by preoperative pathological examination.

7. Treatment

Since the preoperative diagnosis of GIS is often unclear, there is no unified standard for the treatment of schwannomas, but it is clinically believed that the active surgical treatment of schwannomas has been validated. According to the size and location of the tumors and their association with surrounding tissues, common surgical methods include endoscopic resection and laparoscopic and open surgery.

Endoscopic resection is often suggested for tumors <3 cm in diameter (59). Common surgical types include endoscopic mucosal resection (60) and full-thickness endoscopic surgery resection. However, since the tumor grows under the mucosa, the use of endoscopic resection increases the risk of bleeding, perforation and gastrointestinal fistula. There is no clear evidence that endoscopic resection may lead to incomplete tumor resection and recurrence of residual tumor risks such as metastasis. However, in recent years, new technologies for endoscopic resection have been developed, such as extraluminal endoscopic submucosal tunnel resection (61), which has improved the safety and cure rate of endoscopic resection. Endoscopic resection is not recommended for patients with deep locations, unclear tumor boundaries and metastases.

Surgical resection is currently the most effective way to treat GIS. Common surgical methods include simple tumor resection and partial gastric (intestinal) resection. Experts have reached a consensus that tumor lymph node metastases may be rare, so routine lymph node dissection is not recommended. With the development and popularization of laparoscopic technology, the laparoscopic replacement of traditional open surgery has been accepted by an increasing number of clinicians. Laparoscopic and endoscopic cooperative surgery (LECS) refers to the simultaneous application of laparoscopy (hard scope) and endoscopy (soft scope) during an operation (62). LCES makes up for the shortcomings of a single surgical method. Huang et al (63) reported that the endoscopy-assisted laparoscopic resection group was superior to the laparoscopy group, in terms of a shorter operation time, decreased intraoperative bleeding, short postoperative intestinal function recovery time, and a shortened length of hospitalization (P<0.05). For tumors <30 mm in diameter, a modified LECS technique called ‘closed LECS’ was created by Kikuchi et al (59) to avoid the potential risk of gastric contents or tumor cells spilling into the abdominal cavity. Therefore, LECS compensated for the inaccurate positioning of the tumor by single-line laparoscopic surgery or the increased risk of bleeding and perforation caused by single-line endoscopic resection, decreases the contaminated area of the operation, lowers the possibility of luminal stenosis, increases safety and is beneficial for the patient's postoperative recovery.

Due to the large difference between the location and volume of GIS, special surgical methods, such as Billroth II (21), may be used for symptoms such as a unique tumor location, severe obstruction, bleeding, large size and compression of other organs. For individuals with diagnosed GIMS, surgical resection, radiotherapy and chemotherapy are recommended (52).

8. Prognosis

After the long-term follow-up of patients with benign schwannoma, no recurrence was found after complete tumor resection. As suggested by a longitudinal study, GIMS has a poor prognosis, as 3 out of 10 patients died due to the metastasis or recurrence of GIMS within 5 years after surgery (64). Bevacizumab is an anti-vascular endothelial factor monoclonal antibody that has been shown to effectively inhibit tumor development. It is one of the few drugs for the treatment of schwannomas and has been used in vestibular schwannomas (65). Currently, the effectiveness of molecular therapy for GIMS is unclear because of the very low number of reported cases. Further molecular therapy research will be useful for determining its usefulness in the treatment of GIMS.

9. Conclusion

GIS is an uncommon, slow-growing and benign gastrointestinal interstitial tumor that may become malignant in a few cases. Most of these tumors have no obvious specific symptoms or signs. Endoscopy, imaging and ultrasound examinations play a role in differential diagnosis, and biopsy can improve the accuracy of diagnosis. Positivity for S-100 is the gold standard for diagnosing GIS. GIS currently has a relatively high rate of clinical misdiagnosis, resulting in the relatively limited selection of surgical procedures. Complete surgical removal of the tumor is the main method of treatment for GIS. LECS has obvious advantages in the treatment of GIS and is worth recommending.

Glossary

Abbreviations

GIS

gastrointestinal schwannoma

GIMS

gastrointestinal malignant schwannoma

GIST

gastrointestinal stromal tumor

NF1

neurofibromatosis type 1

NF2

neurofibromatosis type 2

EUS-FNA

endoscopic ultrasound-guided fine-needle aspiration

EUS-TCB

endoscopic ultrasound-guided fine-needle aspiration

CT

computed tomography

MRI

magnetic resonance imaging

¹⁸FDG-PET

¹⁸fluorodeoxyglucose positron emission tomography

LECS

laparoscopic and endoscopic cooperative surgery

NSE

neuron-specific enolase

DOG-1

discovered on GIST-1

GFAP

glial fibrillary acidic protein

SMA

smooth muscle antigen

HMB-45

human melanoma black45

LCA

leucocyte common antigen

PCNA

proliferating cell nuclear antigen

Funding Statement

The present study was funded by the Natural Science Foundation of Jilin Province, China (grant no. 20190201085JC).

Funding

The present study was funded by the Natural Science Foundation of Jilin Province, China (grant no. 20190201085JC).

Availability of data and materials

All data sets generated and/or analyzed during the study are available from the authors on reasonable request.

Authors' contributions

WY conceived the main idea and designed and created the main theoretical parts of this review. ZQ, NY and MP contributed to the design and implementation of research and to writing the manuscript. NY and MP searched and filtered references and suggested the contents of tables. ZQ, NY and MP proofread the manuscript and revised the manuscript for intellectual content. WY and ZQ confirmed the authenticity of all the raw data. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.