Immunoglobulin G4-Related Inflammatory Pseudotumor Presenting as a Solitary Mass in the Stomach

Article information

Clin Endosc. 2016;49(2):197-201
Publication date (electronic) : 2016 February 12
doi : https://doi.org/10.5946/ce.2015.074
Department of Internal Medicine, Pusan National University School of Medicine, Busan, Korea
Correspondence: Bong Eun Lee Department of Internal Medicine, Pusan National University School of Medicine and Biomedical Research Institute, Pusan National University Hospital, 179 Gudeok-ro, Seo-gu, Busan 49241, Korea Tel: +82-51-240-7225, Fax: +82-51-254-3127, E-mail: bongsul@hanmail.net
Received 2015 May 4; Revised 2015 June 26; Accepted 2015 July 11.

Abstract

Immunoglobulin G4 (IgG4)-related disease (IgG4RD) is a relatively recently recognized entity that is histopathologically characterized by an extensive infiltration of lymphocytes and IgG4-positive plasma cells with dense fibrosis. IgG4RD is now known to affect any organ system, and a few cases of gastrointestinal lesions have also been reported. However, solitary IgG4RD of the stomach is still very rare. Furthermore, as it can mimic malignant conditions, it is important to recognize this disease to avoid unnecessary surgery. Herein, we present a case of IgG4RD presenting as an isolated subepithelial mass in the stomach.

INTRODUCTION

Immunoglobulin G4 (IgG4)-related disease (IgG4RD) is a relatively recently defined condition that is histologically characterized by an extensive infiltration of lymphocytes and IgG4-positive plasma cells with storiform fibrosis [1]. At present, it is known that various organs can be affected by IgG4RD, including the pancreas, bile duct, gallbladder, liver, lung, salivary gland, retroperitoneum, and gastrointestinal tract [2]. However, isolated IgG4RD of the stomach is still very rare. Here, we report a case of IgG4RD of the stomach presenting as a subepithelial mass without any other organ involvement.

CASE REPORT

A 27-year-old woman presented for the evaluation of high blood pressure. Autosomal dominant polycystic kidney disease was diagnosed on abdominal computed tomography (CT), and she was referred to our gastroenterology clinic for further evaluation of an intramural enhancing mass in the gastric fundus that was incidentally found on the CT scan (Fig. 1). She had no gastrointestinal complaints, and physical examination showed no abnormalities. The laboratory results were unremarkable except for hypocytic and hypochromic anemia (hemoglobin, 10.1 g/dL). She underwent an esophagogastroduodenoscopy. Helicobacter pylori-positive lymphofollicular gastritis was seen, and, macroscopically, a 4-cm subepithelial mass with surface ulceration was found on the fundus (Fig. 2A, B). Endoscopic ultrasonography (EUS) showed a 3.4×1.6 cm well-circumscribed homogeneous hypoechoic mass located mainly in the muscularis mucosa and submucosa (Fig. 2C). Because multiple biopsy specimens only showed chronic ulcer on microscopic examination, laparoscopic wedge resection was performed to rule out tumors with malignant potential such as a neuroendocrine tumor (NET) or gastrointestinal stromal tumor (GIST). Grossly, the resected specimen showed a well-defined whitish-gray solid subepithelial mass (Fig. 3). On microscopic examination, dense fibrosis admixed with inflammatory cells was seen composing the submucosal mass that extended to the subserosa (Fig. 4A). Bland-looking spindle cells were arranged in a storiform pattern in the collagenous stroma (Fig. 4B), and there was a dense infiltration of polymorphous inflammatory cells composed predominantly of plasma cells with a few lymphocytes, eosinophils, and neutrophils (Fig. 4C). These spindle cells showed one to two mitoses per 10 high power fields (HPFs), and positive staining for smooth muscle actin and negative staining for ALK, desmin, CD34, DOG-1, c-kit, and S-100. Additional immunohistochemical staining revealed increased IgG-positive and IgG4-positive plasma cells (402/HPF and 102/HPF, respectively), and the ratio of IgG4+/IgG+ plasma cells was 25.3% (Fig. 4D, E). Because these pathological features were compatible with IgG4RD, and there was no evidence of any other organ involvement, isolated gastric IgG4RD was finally diagnosed. The serum IgG and IgG4 levels were not elevated (1,012 and 295 mg/L, respectively). She was discharged without significant postoperative complications, and there has been no evidence of disease recurrence during the 1-year follow-up period.

Fig. 1.

Abdominal computed tomography images showing multiple cysts in both kidneys (A) and an intramural enhancing mass in the gastric fundus (B).

Fig. 2.

Endoscopic findings. (A) Helicobacter pylori-positive lymphofollicular gastritis. (B) An approximately 4-cm, hard, fixed subepithelial mass with distinct ulceration on the surface, located in the fundus. (C) Endoscopic ultrasonography image showing a 3.4×1.6 cm homogeneous hypoechoic mass located in the muscularis mucosa up to the submucosa.

Fig. 3.

Gross findings after formalin fixation. (A, B) On the specimen section, a well-defined homogeneous gray-white solid submucosal mass (asterisks) is identifiable. The gastric mucosa (arrows) is unremarkable.

Fig. 4.

Pathologic findings. (A) Dense fibrosis admixed with inflammatory cells composing the submucosal mass that extends to the subserosa (asterisk, mucosa; arrowhead, submucosa; circle, muscularis propria; H&E stain, ×12.5). (B) Bland-looking spindle cells arranged in a storiform pattern (H&E, ×200). (C) Fibroblastic cells admixed with dense lymphoplasmacytic cells (H&E, ×400). (D) Immunoglobulin G (IgG) immunohistochemical staining showing increased numbers of IgG-positive plasma cells in the stroma (402/high power field [HPF], ×200). (E) IgG4 immunohistochemical staining revealing increased numbers of IgG4-positive plasma cell infiltration (102/HPF, ×200); the ratio of IgG4+/IgG+ plasma cells was 25.3%.

DISCUSSION

IgG4RD was first proposed as a new clinicopathological entity by Kamisawa et al. [3] in 2003 as a multisystemic disease in patients with autoimmune pancreatitis. IgG4RD is histologically defined as an intensive infiltration of IgG4-positive plasma cells and T-lymphocytes with storiform fibrosis, and clinically known to respond well to steroids [1]. Multiple organs can be affected synchronously or metachronously, including the pancreas, biliary tree, liver, kidneys, salivary gland, orbit, breast, pericardium, aorta, skin, lungs, prostate, meninges, retroperitoneum, and gastrointestinal tract [2]. Recently, many cases of IgG4RD affecting organs other than the pancreas have been reported, such as IgG4-related inflammatory pseudotumors of the liver [4], lungs [5], and greater omentum [6] with or without autoimmune pancreatitis, and isolated IgG4RD seems to have been increasingly detected owing to an increased awareness of this disease entity.

However, IgG4RD in the stomach is still rare. On the basis of the eight cases reported thus far, the gastric manifestations of this disease seem to consist of two types: polypoid mass-like (six cases) or ulcerative (two cases) lesions (Table 1). Rollins et al. [7] first described 5 to 6 cm gastric IgG4-related pseudotumors with no evidence of any other organ involvement as confirmed with laparoscopic resection. Chetty et al. [8] reported two patients with gastric sclerosing nodular IgG4RD that was diagnosed on surgical resection. Thereafter, Na et al. [9] reported an 8-mm gastric nodular IgG4RD confirmed with endoscopic submucosal dissection, and Kim et al. [10] described two cases of IgG4-related inflammatory pseudotumors in the stomach, in which EUS showed a well-defined homogeneous hypoechoic mass arising from echo layer 4 (muscularis propria). On the other hand, two patients presented with chronic gastric ulcerations. Fujita et al. [11] reported a case with refractory gastric ulcers that worsened after standard proton pump inhibitor therapy and H. pylori eradication, and similarly Bateman et al. [12] described a case of intractable gastric ulcer showing storiform fibrosis and abundant infiltration of IgG4-positive plasma cells. Of a total of eight cases reported, only one case of ulcerative-type IgG4RD was possible to confirm by using conventional endoscopic biopsy with elevated serum IgG4 levels. For the remaining seven cases, the patients had to undergo surgical or endoscopic resection for the final diagnosis, and their serum IgG4 levels were within the reference range. In this regard, Na et al. [9] suggested that predominant inflammatory infiltrates of IgG4RD in the gastric submucosa while sparing the mucosa seem to make the diagnosis difficult. Furthermore, endoscopic and radiographic difficulties in distinguishing IgG4RD from other malignancies or tumors with malignant potential are also reasons for a troublesome diagnosis. These situations lead to a higher possibility of unnecessary surgery in these patients, although IgG4RD is a medically treatable condition that responds well to steroid therapy.

Clinicopathological Features of Gastric Immunoglobulin G4-Related Disease

In our case, macroscopically, a 4-cm subepithelial mass with surface ulceration was incidentally found on the fundus, and EUS revealed a well-circumscribed homogeneous hypoechoic mass located mainly in the muscularis mucosa and submucosa. Although endoscopic biopsy failed to detect the disease, we considered laparoscopic wedge resection to rule out a NET or GIST without doubt. After obtaining the final diagnosis and reviewing similar cases in which patients had undergone unnecessary surgery, we learned that clinical awareness and suspicion of IgG4RD is the most important factor in diagnosing this disease entity. Although H. pylori-associated gastritis was seen in our case, there has been no evidence of a link between IgG4RD and H. pylori infection thus far.

In conclusion, isolated gastric IgG4RD is very rare. Because it is difficult to endoscopically differentiate IgG4RD from other potentially malignant tumors and to definitively identify the disease with conventional endoscopic biopsy, it is most important to recognize this disease entity to avoid unnecessary surgery. Because IgG4RD is known to respond well to steroids, it is important to attempt to confirm the disease before considering invasive surgery. Furthermore, we suggest considering IgG4RD in the differential diagnosis in the presence of a gastric subepithelial mass that has a homogeneous hypoechoic feature on EUS.

Notes

Conflicts of Interest: The authors have no financial conflicts of interest.

Acknowledgements

This work was supported by the year 2014 clinical research grant from Pusan National University Hospital.

References

1. Umehara H, Okazaki K, Masaki Y, et al. Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011. Mod Rheumatol 2012;22:21–30.
2. Stone JH, Zen Y, Deshpande V. IgG4-related disease. N Engl J Med 2012;366:539–551.
3. Kamisawa T, Funata N, Hayashi Y, et al. A new clinicopathological entity of IgG4-related autoimmune disease. J Gastroenterol 2003;38:982–984.
4. Kanno A, Satoh K, Kimura K, et al. Autoimmune pancreatitis with hepatic inflammatory pseudotumor. Pancreas 2005;31:420–423.
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Article information Continued

Fig. 1.

Abdominal computed tomography images showing multiple cysts in both kidneys (A) and an intramural enhancing mass in the gastric fundus (B).

Fig. 2.

Endoscopic findings. (A) Helicobacter pylori-positive lymphofollicular gastritis. (B) An approximately 4-cm, hard, fixed subepithelial mass with distinct ulceration on the surface, located in the fundus. (C) Endoscopic ultrasonography image showing a 3.4×1.6 cm homogeneous hypoechoic mass located in the muscularis mucosa up to the submucosa.

Fig. 3.

Gross findings after formalin fixation. (A, B) On the specimen section, a well-defined homogeneous gray-white solid submucosal mass (asterisks) is identifiable. The gastric mucosa (arrows) is unremarkable.

Fig. 4.

Pathologic findings. (A) Dense fibrosis admixed with inflammatory cells composing the submucosal mass that extends to the subserosa (asterisk, mucosa; arrowhead, submucosa; circle, muscularis propria; H&E stain, ×12.5). (B) Bland-looking spindle cells arranged in a storiform pattern (H&E, ×200). (C) Fibroblastic cells admixed with dense lymphoplasmacytic cells (H&E, ×400). (D) Immunoglobulin G (IgG) immunohistochemical staining showing increased numbers of IgG-positive plasma cells in the stroma (402/high power field [HPF], ×200). (E) IgG4 immunohistochemical staining revealing increased numbers of IgG4-positive plasma cell infiltration (102/HPF, ×200); the ratio of IgG4+/IgG+ plasma cells was 25.3%.

Table 1.

Clinicopathological Features of Gastric Immunoglobulin G4-Related Disease

Case no. Study Sex/Age (yr) Endoscopic finding Location EUS finding Diagnostic procedure Involved layer
1 Rollins et al. (2011) [7] F/75 Polypoid mass, 5 cm Mid-body, great curvature NA WR SM
2 Chetty et al. (2011) [8] F/45 Nodule, 1.5 cm Fundus NA WR SM
3 Chetty et al. (2011) [8] M/60 Multiple nodules, up to 2.2 cm Antrum and pylorus NA DG MP to SS
4 Na et al. (2012) [9] M/56 Nodule, 8 mm Lower body, lesser curvature NA ESD SM
5 Kim et al. (2012) [10] F/59 Subepithelial mass, 3.3 cm Mid-body, great curvature Homogeneous, hypoechoic mass arising from echo layer 4 WR NA
6 Kim et al. (2012) [10] F/54 Fixed mass, 2.1 cm NA Homogeneous, hypoechoic mass arising from echo layer 4 WR SS
7 Present study F/27 Subepithelial mass with surface ulceration, 4 cm Fundus Homogeneous, hypoechoic mass located in the muscularis mucosa up to the submucosa WR SM to SS
8 Fujita et al. (2010) [11] F/73 Ulcer, 3 cm Lower body, lesser curvature NA DG SM to SS
9 Bateman et al. (2012) [12] M/77 Ulcer, diffuse Body NA Biopsy Mucosa (only the mucosa was examined)

EUS, endoscopic ultrasonography; NA, not available; WR, wedge resection; SM, submucosa; DG, distal gastrectomy; MP, muscularis propria; SS, subserosal; ESD, endoscopic submucosal dissection.