Gastric Angiolipoma: A Rare Entity.
CLINICAL AND ENDOSCOPIC FEATURES
Angiolipomas generally present as encapsulated subcutaneous tumors. They are usually smaller than 2 cm in diameter, and young adult patients typically present with multiple tender masses in the arms and trunk. (12) Gastrointestinal (GI) angiolipoma is rare, and to the best of our knowledge, only 4 angiolipoma cases have been reported in the stomach so far (Table). (4-7) Occasional cases have been reported in other areas of the GI tract, including the esophagus, (13) duodenum, (8,14) small intestine, (15,16) colon, (9,11,17-19) and rectum. (20,21) Angiolipoma in the GI tract almost exclusively occurs as a solitary lesion and usually lacks specific clinical manifestations. Patients may be asymptomatic, or some may present with ulcerative GI bleeding and anemia, or symptoms of obstruction or intussusception due to the increasing size of the tumor. In the 4 reported gastric angiolipoma case reports, 3 presented with GI hemorrhage and anemia (4-6) and 1 with intussusception caused by synchronous occurrence of a large solitary gastric Peutz-Jeghers polyp (Table). (7) Hemorrhage is generally attributed to the proliferating vessels or due to the ulcer.
The antrum appears to be the most common site for gastric angiolipomas. Upper GI endoscopy typically shows submucosal polypoid mass with superficial ulceration, probably due to the mass effect of the expanding lesion (Figure 1). (4-6)
Angiolipoma appears as a mass with a central hyperechoic portion surrounded by a hypoechoic part on the periphery on abdominal echo. (5,11) Endoscopic ultrasound can show isoechoic and hyperechoic parts, probably in part secondary to the stromal fibrosis induced by ulceration. (5) Abdominal computed tomography (CT) can show variable findings. Usually gastric angiolipoma on CT has a heterogenous appearance, (13) with mixed fat and soft tissue density, raising a radiologic concern for mixed mesenchymal tumors or intratumoral hemorrhage (Figure 2). It appears as a low and isodense lesion on the pre-enhanced CT, but it could appear as a high-density mass in the post-enhanced CT because of its lipomatous component. However, because the overall density of the lesion on CT can vary according to the proportion of different components, nonenhancement may also be seen. (5) Thus, the CT findings are not entirely specific and may not be very helpful to distinguish it from other subepithelial lesions. Magnetic resonance imaging typically shows a fat signal intensity mass with areas of low signal intensity on T1-weighted and high signal intensity on T2-weighted images, and intense enhancement representing the vascular component of the lesion. (22)
Not surprisingly, the overall preoperative diagnostic accuracy for gastric angiolipoma is not very high, given the rarity of the neoplasm coupled with the nonspecific clinical presentation and lack of specific findings on imaging studies.
The size of reported gastric angiolipoma ranges from 0.5 up to 5 cm (Table). (4-7) Grossly, angiolipoma is a well-circumscribed, encapsulated lesion, the cut surface of which varies from yellow to red according to the prevalence of fat or vascular component. The surface of the tumor may demonstrate brownish-red erosion. Angiolipoma can be classified by the ratio of adipose and vascular tissue components as predominantly lipomatous or angiomatous type. Histologically, gastric angiolipoma is circumscribed and pretty much encapsulated, and is composed of mature adipose tissue with an interspersed vascular proliferation (Figures 3 to 6). Additionally, these lesions often ulcerate into the overlying mucosa, along with active inflammation and reactive epithelial changes with fibrinopurulent exudate (Figure 4). In contrast to cutaneous angiolipomas, an interesting histologic feature of gastric angiolipoma and many other nonsubcutaneous angiolipomas is the absence of fibrin thrombi (Figure 5). Therefore, the presence of fibrin thrombi is not a required diagnostic criterion for nonsubcutaneous angiolipomas. The reason for this histologic difference between subcutaneous and nonsubcutaneous angiolipomas remains unclear. The external location of the subcutaneous angiolipomas and the largely peripheral location of the fibrin thrombi in these tumors suggest that physical irritation may be a contributory factor. (6)
Given the predominant submucosal location of the neoplasm, a preoperative biopsy specimen mostly is limited to superficial mucosa and likely shows nonspecific features, including ulcer without lesional tissue. Hence, the accurate diagnosis of gastric angiolipomas is often made on final surgical pathology examination of the excised specimen.
Angiolipoma is typically diagnosed with hematoxylineosin stain, and immunohistochemistry is rarely, if ever, needed. Angiolipoma shows focal to diffuse positivity for S100 protein in the adipocytes as well as positivity for endothelial markers (eg, CD34 and CD31) in the vascular component. Cytogenetically, angiolipoma is almost unique among adipocytic neoplasms because, with a single exception, all tumors investigated cytogenetically have had a normal karyotype. (23) This suggests that the pathogenesis of angiolipoma may be different from that of ordinary lipoma. Angiolipoma seems to show aberrant expression of full-length HMGA2, although at levels lower than in lipoma with 12q rearrangements. (24)
The differential diagnosis may include some benign and malignant gastric neoplasms, such as nonneoplastic gastric polyps; some other soft tissue tumors with lipomatous components/differentiation, such as lipoma, angiomyolipoma, and well-differentiated liposarcoma; and vascular lesions, such as angiodysplasia and glomus tumors. (25)
Nonneoplastic submucosal gastric lesions include inflammatory fibroid polyp. Inflammatory fibroid polyp exhibits a submucosal proliferation of bland spindle-shaped cells, prominent vessels, and inflammatory cells "typically" rich in eosinophils dispersed in a fibromyxoid stroma. "Onion-skinning" characterized by a concentric proliferation of bland lesional spindle cells around blood vessels is often seen. The lesional cells are immunoreactive for CD34. Other gastric polyps, including hyperplastic polyp and fundic gland polyp, are less likely in the differential because these are predominantly "mucosal-based" polyps. Additionally, hyperplastic polyps show elongated, distorted, and branched foveolar glands in a background of edematous and inflamed lamina propria. Fundic gland polyps have a proliferation of small and dilated glands lined by cytologically bland parietal and chief cells.
Other soft tissue tumors with lipomatous differentiation may demonstrate gross and/or endoscopic features similar to those of angiolipoma. Definitive diagnosis often relies on histopathologic examination. Unlike angiolipoma, lipoma lacks vascular components, whereas angiomyolipoma additionally shows lesional spindle or epithelioid-appearing cells along with thick-walled blood vessels and is immunoreactive for HMB-45 and MART-1, and shows variable staining for smooth muscle actin. Another main differential diagnosis would be well-differentiated liposarcoma, which is characterized by atypical, often multinucleated adipocytes and lipoblasts admixed with mature, uniform adipocytes with thick fibrous septa. Typically, angiolipoma does not demonstrate the cytologic atypia usually seen in well-differentiated liposarcoma. (26) As ancillary tools, MDM2 and CDK4 are becoming increasingly popular immunohistochemical markers for well-differentiated liposarcomas because they are essentially never overexpressed in benign lipomas. (27) Karyotypic analysis has shown that well-differentiated liposarcoma is characterized by the presence of ring or giant marker chromosomes. (27) Concomitant amplification of MDM2, CDK4, and HMGA2, as well as overexpression of the encoded proteins, is characteristic of well-differentiated liposarcomas. (27) The high specificity and sensitivity of detection of MDM2 and CDK4 amplification by using fluorescent in situ hybridization have been shown to be powerful tools for separating well-differentiated liposarcomas from benign lipomatous lesions. (28)
Other vascular lesions, such as angiodysplasia, can be distinguished from angiolipoma because the former do not contain appreciable adipose tissue and do exhibit a proliferation of small, dilated, and distorted thin-walled blood vessels with focal mucosal extension. Glomus tumors show abundant dilated, thin-walled blood vessels, are lined by a single layer of endothelial cells, and are surrounded by nests of uniform and round glomus cells, which are strongly positive for smooth muscle actin and vimentin.
PROGNOSIS AND TREATMENT
Angiolipoma is considered to be universally benign, with no malignant counterpart described in the literature. Complete surgical excision is recommended to avoid recurrences. Once completely excised, these neoplasms typically do not recur.
Gastric angiolipoma is a rare entity, which can present as chronic GI bleeding and anemia or obstructive symptoms. These are benign lesions with no propensity for local recurrence or aggressive behavior, and hence the clinical significance lies in being aware of this entity, being aware of its characteristic histologic features in the stomach, and distinguishing it from other benign and malignant neoplasms that may come in the clinical and/or radiologic differential diagnosis.
Please Note: Illustration(s) are not available due to copyright restrictions.
We thank Thomas Dykes, MD, for the radiologic image (Figure 2).
(1.) Howard WR, Helwig EB. Angiolipoma. Arch Dermatol. 1960; 82:924-931.
(2.) Lin JJ, Lin F. Two entities in angiolipoma: a study of 459 cases of lipoma with review of literature on infiltrating angiolipoma. Cancer. 1974; 34(3):720-727.
(3.) Dixon AY, McGregor DH, Lee SH. Angiolipomas: an ultrastructural and clinicopathological study. Hum Pathol. 1981; 12(8):739-747.
(4.) DeRidder PH, Levine AJ, Katta JJ, Catto JA. Angiolipoma of the stomach as a cause of chronic upper gastrointestinal bleeding. Surg Endosc. 1989; 3(2):106-108.
(5.) Nam YH, Park SC, Kim HJ, et al. Angiolipoma of the stomach presenting with anaemia. Prz Gastroenterol. 2014; 9(6):371-374.
(6.) McGregor DH, Kerley SW, McGregor MS. Case report: gastric angiolipoma with chronic hemorrhage and severe anemia. Am J Med Sci. 1993; 305(4):229-235.
(7.) Hunt J, Tindal D. Solitary gastric Peutz-Jeghers polyp and angiolipoma presenting as acute haemorrhage. Aust N Z J Surg. 1996; 66(10):713-715.
(8.) Jung IS, Jang JY, Ryu CB, et al. Angiolipoma of the duodenum diagnosed after endoscopic resection. Endoscopy. 2004; 36(4):375.
(9.) Okuyama T, Yoshida M, Watanabe M, Kinoshita Y, Harada Y. Angiolipoma of the colon diagnosed after endoscopic resection. Gastrointest Endosc. 2002; 55(6):748-750.
(10.) Ferrozzi F, Tognini G, Bova D, Pavone P. Lipomatous tumors of the stomach: CT findings and differential diagnosis. J Comput Assist Tomogr. 2000; 24(6):854-858.
(11.) Chen YY, Soon MS. Preoperative diagnosis of colonic angiolipoma: a case report. World J Gastroenterol. 2005; 11(32):5087-5089.
(12.) Rogy MA, Mirza D, Berlakovich G, Winkelbauer F, Rauhs R. Submucous large-bowel lipomas-presentation and management: an 18-year study. Eur J Surg. 1991; 157(1):51-55.
(13.) Jensen EH, Klapman JB, Kelley ST. Angiolipoma of the esophagus: a rare clinical dilemma. Dis Esophagus. 2006; 19(3):203-207.
(14.) Mohl W, Fischinger J, Moser C, Remberger K, Zeuzem S, Stallmach A. Duodenal angiolipoma-endoscopic diagnosis and therapy. Z Gastroenterol. 2004; 42(12):1381-1383.
(15.) Della VN, Bianco L, Bonuso C, Annecchiarico M, Di SP, Caiazza A. Rare ileal localisation of angiolipoma presenting as chronic haemorrhage and severe anaemia: a case report. J Med Case Rep. 2008; 2:129.
(16.) Aminian A, Noaparast M, Mirsharifi R, et al. Ileal intussusception secondary to both lipoma and angiolipoma: a case report. Cases J. 2009; 2:70-99.
(17.) Kato K, Matsuda M, Onodera K, Sakata H, Kobayashi T, Kasai S. Angiolipoma of the colon with right lower quadrant abdominal pain. Dig Surg. 1999; 16(5):441-444.
(18.) Maesawa C, Tamura G, Sawada H, Kamioki S, Nakajima Y, Satodate R. Angiomyolipoma arising in the colon. Am J Gastroenterol. 1996; 91(9): 1852-1854.
(19.) Molinares B, Goldstein A, Varela GJ, Mesa S. Colonic angiolipoma-a rare finding in the gastrointestinal tract: case report and review of literature. J Radiol Case Rep. 2012; 6(6):23-28.
(20.) Kacar S, Kuran S, Temucin T, Odemis B, Karadeniz N, Sasmaz N. Rectal angiolipoma: a case report and review of literature. WorldJ Gastroenterol. 2007; 13(9):1460-1465.
(21.) Ishizuka M, Nagata H, Takagi K, Horie T, Abe A, Kubota K. Rectal angiolipoma diagnosed after surgical resection: a case report. World J Gastroenterol. 2007; 13(3):467-469.
(22.) Moukaddam H, Pollak J, Haims AH. MRI characteristics and classification of peripheral vascular malformations and tumors. Skeletal Radiol. 2009; 38(6): 535-547.
(23.) Sciot R, Akerman M, Dal CP, et al. Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group. Am J Surg Pathol. 1997; 21(4):441-444.
(24.) Bartuma H, Panagopoulos I, Collin A, et al. Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups. Mol Cancer. 2009; 8:36.
(25.) Lindeberg M. Diagnostic Pathology: Soft Tissue Tumors. 2nd ed. Philadelphia, PA: Elsevier; 2015.
(26.) Fenoglio-Preiser CM, Noffsinger AE, Stemmermann GN, Lantz PE, Isaacson PG. Gastrointestinal Pathology: An Atlas and Text. 3rd ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2008.
(27.) Hornick JL. Practical Soft Tissue Pathology: A Diagnostic Approach: A Volume in the Pattern Recognition Series. 1st ed. Philadelphia, PA: Saunders; 2013.
(28.) Shimada S, Ishizawa T, Ishizawa K, Matsumura T, Hasegawa T, Hirose T. The value of MDM2 and CDK4 amplification levels using real-time polymerase chain reaction for the differential diagnosis of liposarcomas and their histologic mimickers. Hum Pathol. 2006; 37:1123-1129.
Yong-Jun Liu, MD, PhD; Dipti M. Karamchandani, MD
Accepted for publication September 15, 2016.
From the Department of Pathology, Penn State Milton S. Hershey Medical Center & Penn State College of Medicine, Hershey, Pennsylvania.
The authors have no relevant financial interest in the products or companies described in this article.
Reprints: Dipti M. Karamchandani, MD, Division of Anatomic Pathology, Department of Pathology, Penn State Milton S. Hershey Medical Center, 500 University Dr, H179, Hershey, PA 17033-0850 (email: firstname.lastname@example.org).
Caption: Figure 1. Endoscopic examination shows a polypoid and focally ulcerating, partially circumferential submucosal-based mass.
Caption: Figure 2. Abdominal computed tomography shows a stomach mass with mixed fat and soft tissue density, raising a concern for intratumoral hemorrhage or rare lesion, such as mixed mesenchymal tumor or a liposarcoma.
Caption: Figure 3. Low-power photomicrograph of gastric angiolipoma showing the overlying gastric antral mucosa and the submucosal proliferation of mature adipose tissue and blood vessels (hematoxylin-eosin, original magnification X20).
Caption: Figure 4. Low-power photomicrograph highlighting the gastric angiolipoma ulcerating into the overlying gastric antral mucosa. Associated fibrinopurulent exudate and reactive epithelial changes can be seen (hematoxylin-eosin, original magnification X20).
Caption: Figure 5. Photomicrograph highlighting the proliferating blood vessels in gastric angiolipoma. Note the absence of fibrin thrombi in the gastric angiolipoma, in contrast to the subcutaneous angiolipomas (hematoxylin-eosin, original magnification X100).
Caption: Figure 6. Photomicrograph highlighting the mature adipose tissue component in gastric angiolipoma (hematoxylin-eosin, original magnification X100).
Summary of the 4 Gastric Angiolipoma Case Reports Case No. Age, Size Location (Source) y/Sex 1 (DeRidder 59/Male 0.5-0.6 cm Gastric body et al (4)) in diameter 2 (Nam et al 69/Male 5 x 4 x 2 cm Gastric antrum (5)) 3 (McGregor 58/Female 1.6 x 1.5 x Gastric antrum et al (6)) 1.4 cm 4 (Hunt and 27/Female 5 cm in diameter Distal stomach Tindal (7)) (overridden by a 8.0 x 5.5 x 4.5 cm Peutz-Jeghers-type polyp) Case No. Clinical Presentation Imaging Findings (Source) 1 (DeRidder Occasionally passed Not available et al (4)) black stools 2 (Nam et al 2 wk of shortness of Not available (5)) breath with chronic hemorrhage and anemia (Hb: 6.0 g/dL) 3 (McGregor 1 mo of melena and CT: submucosal et al (6)) epigastric discomfort cystic lesion with (Hb: 5.1 g/dL) diffuse fluid density without enhancement after contrast EUS: isoechoic lesion at the third echo layer with the echogenic portion at the luminal side of the lesion 4 (Hunt and 6 wk of vomiting and Not available Tindal (7)) 8 kg of weight loss Case No. Postoperative Course (Source) 1 (DeRidder The patient maintained normal Hb during a et al (4)) 12-mo follow-up period 2 (Nam et al The patient maintained normal Hb without (5)) subsequent gastrointestinal symptoms during a 2.5-y follow-up period 3 (McGregor The patient had done well postoperatively et al (6)) 4 (Hunt and Postoperative recovery was without incident Tindal (7)) Abbreviations: CT, computed tomography; EUS, endoscopic ultrasound; Hb, hemoglobin.
|Printer friendly Cite/link Email Feedback|
|Title Annotation:||Resident Short Reviews|
|Author:||Liu, Yong-Jun; Karamchandani, Dipti M.|
|Publication:||Archives of Pathology & Laboratory Medicine|
|Date:||Jun 1, 2017|
|Previous Article:||The Significance of Lymphovascular Invasion of the Spermatic Cord in the Absence of Cord Soft Tissue Invasion.|
|Next Article:||Chondroblastoma: An Update.|