Protruding Lesions

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Jpn J Radiol (2016) 34:321–330

DOI 10.1007/s11604-016-0534-6

PICTORIAL ESSAY

The imaging features of protruding esophageal lesions


Hayato Tomita1 · Kunihisa Miyakawa1 · Shinji Wada1 · Satoko Okamoto1 ·
Tsuyoshi Morimoto1 · Keiko Kishimoto1 · Yasuo Nakajima1 

Received: 24 January 2016 / Accepted: 29 February 2016 / Published online: 11 March 2016
© Japan Radiological Society 2016

Abstract  Except for squamous cell carcinoma and ade- Esophagography includes single-contrast and double-con-
nocarcinoma, lesions that protrude into the esophagus are trast views. Double-contrast esophagography is performed
rare, and include benign and malignant tumors. The imag- to evaluate the mucosal contour and thus the extent of
ing findings of these lesions on esophagography, computed protrusion of esophageal lesions. CT and magnetic reso-
tomography (CT), and magnetic resonance imaging (MRI) nance imaging (MRI) are useful to characterize tissues
are often non-specific. However, some of them reveal and for staging. The most important diagnostic challenge
characteristic imaging findings. In addition, esophagogra- is to differentiate esophageal lesions requiring treatment
phy, CT, and MRI are useful to evaluate location, extent, from those that do not; in particular, asymptomatic benign
invasion, vascularity, lymphadenopathy, and metastasis. esophageal lesions are simply followed closely. These radi-
Knowledge of the imaging features of protruding esopha- ological imaging techniques also help to determine whether
geal lesions helps to narrow the differential diagnosis. a biopsy is necessary for benign esophageal lesions. There-
We describe the main features of esophageal protruding fore, radiologists are required to be familiar with these clin-
lesions. ical and imaging features. The purpose of this article is to
discuss and illustrate the features of protruding esophageal
Keywords  Protruding esophageal lesions · Esophagus lesions.
tumors · Esophagography · CT · MRI

Malignant tumors and potentially malignant


Introduction tumors

Protruding esophageal lesions result from a wide spectrum SCC and adenocarcinoma


of esophageal diseases. Patients with esophageal lesions
present with non-specific symptoms, including dysphagia, Esophageal squamous cell carcinoma (SCC) and adenocar-
odynophagia, or chest pain. These lesions are often discov- cinoma account for 90 % of esophageal malignant tumors
ered by endoscopy, esophagography, and computed tomog- [1]. Esophageal SCC is a malignant epithelial tumor origi-
raphy (CT). Endoscopic biopsy and endoscopic ultrasound- nating from epidermal keratinocytes. Esophageal adeno-
guided fine-needle aspiration are the gold standard tests carcinoma arises from a malignant degeneration of Barrett
for making the definitive diagnosis of esophageal tumors. epithelium.
Esophagography has a sensitivity of 90 % for identi-
fication of esophageal cancer [1]. On esophagography,
* Hayato Tomita esophageal SCC or adenocarcinomas appear as a bulky and
m04149@yahoo.co.jp infiltrating mucosal mass with ulcerations and an irregular
1 esophageal wall that has invaded the submucosa. Although
Department of Radiology, St. Marianna University School
of Medicine, 2‑16‑1 Sugao, Miyamae‑ku, Kawasaki, imaging features of esophageal SCC may mimic those of
Kanagawa 216‑8511, Japan adenocarcinoma, adenocarcinoma is more likely to arise

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322 Jpn J Radiol (2016) 34:321–330

Fig. 2  Esophageal adenocarcinoma in a 47-year-old man. Barium


esophagography shows the intraluminal bulky mass and the irregular
surface of the lower esophagus

Fig. 1  Esophageal SCC in a 74-year-old man. a Barium esophagog-


raphy shows the bulky and ulcerative mass with the irregular esopha- Fig. 3  Esophageal carcinosarcoma in a 71-year-old woman. Barium
geal wall in the middle esophagus. b Contrast-enhanced CT shows esophagography shows the intraluminal polypoid filling defect with
the circumferentially thickened wall of the esophagus. Enlarged the smooth esophageal wall in the middle esophagus
lymph node in the mediastinum is evident (arrow)

Carcinosarcoma
in the distal esophagus and invade the stomach. Cross-
sectional CT and MRI are helpful in evaluating staging Carcinosarcoma is a rare malignant tumor composed of
issues associated with mediastinal invasion, metastasis, and both epithelial and mesenchymal tissues. The invasion
lymph node involvement (Figs. 1, 2) [2]. depth in 80 % of esophageal carcinosarcomas is not greater

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Jpn J Radiol (2016) 34:321–330 323

Fig. 4  Esophageal melanoma in a 70-year-old man. Barium esoph-


agography shows the bulky intraluminal filling defect with less irreg-
ular esophageal wall. The shape at the upper edge is obtuse

than the esophageal wall. However, the 5-year survival rate


is not significantly different than that for esophageal SCC
[3].
Most esophageal carcinosarcoma arises in the middle
or lower esophagus. While esophagography demonstrates
a bulky and polypoid intraluminal lesion with an average
diameter of 8 cm, the esophageal wall is smooth because
there is less invasion (Fig. 3). Esophagography may reveal
the cupola sign, a domed shape at the upper edge [2]. The
appearance of carcinosarcoma with predominant sarcoma-
tous components is polypoid due to the presence of few
stroma; in contrast, the appearance with predominant carci-
nomatous components is ulcerative [4]. CT is performed to
evaluate the extent of invasion and metastasis.
Fig. 5  Esophageal GIST in a 67-year-old woman. a Barium esoph-
Melanoma agography shows the extrinsic compression without obstruction at the
lower esophagus. The edge of the bulky mass is obtuse. b Coronal
Primary malignant melanoma of the esophagus (PMME) contrast-enhanced CT shows a heterogeneous mass with a smooth
surface
is also a rare malignant esophageal tumor. PMME can be
diagnosed based on immunohistochemical studies, such as
for HMB45, Melan A, and S-100. on T1-weighted images (T1WI), due to paramagnetic
The location of PMME is in the middle or lower esoph- metal scavenging by melanin, esophageal melanoma rarely
agus due to the high melanocyte content of these cells. exhibits this effect [5].
Esophagography reveals a bulky and lobular tumor with
less irregularity of the esophageal wall, growing radially GIST
and horizontally (Fig. 4). PMME lesions have a smooth
surface and an obtuse shape due to originating from the Gastrointestinal stromal tumor (GIST) is the most com-
submucosa. Although melanoma lesions containing more mon mesenchymal tumor of the gastrointestinal tract.
than 10 % melanin cells appear as hyper-intensity areas GIST, originating from Cajal cells, consists of spindle and

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324 Jpn J Radiol (2016) 34:321–330

epithelioid cells. Immunohistochemical staining is positive Leiomyoma is a submucosal encapsulated tumor consisting
for CD117 (c-KIT) and CD34 in approximately 95 % and of intersecting bands of fibrous tissue and muscle [2].
negative for S-100 in 100 % of cases [6]. Esophageal GIST Leiomyoma locates in the middle or the distal third of the
is known to have malignant potential. esophagus, and is related to the amount of smooth muscle
Esophageal GIST frequently involves the lower third of present. Esophagography shows smooth and crescent defects
the esophagus [2]. Esophagography demonstrates a smooth with right or slightly obtuse angles [2]. On CT, larger esopha-
intraluminal or ulcerative mass with an exophytic compo- geal leiomyomas may become lobular or horseshoe-shaped,
nent [6]. CT detects a well-circumscribed and heterogenous surrounding the esophagus circumferentially. The characteris-
mass with cystic or necrotic components (Fig. 5). The solid tic CT finding of this lesion is an area of iso- or hypo-attenua-
component of GIST typically is hypo-intense on T1WI, tion to muscle, containing areas of calcification (Fig. 8). Cal-
similar to muscle, and slightly hyper-intense on T2WI [7]. cification also occurs in esophageal GIST and old esophageal
Hemorrhage within these lesions is seen, depending on the tuberculosis lesions, and hemangioma. MRI usually reveals a
time course. submucosal mass with hypo- to iso-intensity on T2WI.

Schwannoma Hemangioma and blue rubber bleb nevus syndrome

Esophageal schwannoma is an extremely rare submucosal Esophageal hemangioma results from congenital intrinsic
tumor originating from Schwann cells of the peripheral or acquired vascular occlusion. Osler–Weber–Rendu dis-
nerve sheath. The diagnosis of esophageal schwannoma is ease, Klippel–Trenaunay syndrome, or congenital blue rub-
made by positive immunohistochemical staining for S-100 ber bleb nevus syndrome (BRBNS) can give rise to multiple
and negative staining for histologic smooth muscle markers hemangiomas. BRBNS is a rare congenital disease charac-
such as desmin, actin, and CD-34 [8]. terized by multiple venous malformations involving skins,
Esophageal schwannomas usually arise in the upper or gastrointestinal tract, and other several organs. Although
mid-esophagus. Esophagography reveals a smooth pro- most cases of BRBNS are sporadic, autosomal dominant
truded filling defect. These appear as a homogenous mass inheritance has been reported in some families [10].
on contrasted-enhanced CT; this finding is helpful to dif- Esophagography provides information regarding the
ferentiate esophageal schwannoma from other esophageal size, location, and number, confirmed as lobulated filling
submucosal tumors that are heterogenous [8]. Coronal CT defects. BRBNS based on esophagography may be mis-
and MRI may demonstrate the fusiform shape formed by diagnosed as polyposis syndrome including Peutz–Jegh-
tubular nerves at the upper and lower edges (Fig. 6). ers syndrome, Gardner syndrome, and Cronkhite–Canada
syndrome (Fig. 9) [10]. CT is useful to evaluate phleboliths
Granular cell tumors within the gastrointestinal lesions and the complications, in
particular intussusception and active bleeding. The tumor
Esophageal granular cell tumors are secondary non-epi- demonstrates hyper-intensity on T2WI (Fig. 10). Fluid–
thelial tumors in the esophagus, consisting of ovoid or fluid levels and fat can be also identified in hemangiomas.
polygonal cells containing eosinophilic cytoplasm granules Dynamic contrast-enhanced CT and MRI reveal a periph-
that are separated by collagen bundles. In 1–3 % of cases, eral enhancement in the portal venous phase and a homog-
malignancy develops, with less than 35 % 5-year survival enous enhancement in the late phase [10].
[9].
Esophagography shows a submucosal tumor with trap- Duplication cyst
ezoidal protrusion in the lower third of the esophagus
(Fig.  7). CT and MRI demonstrate a non-specific tumor Duplication cyst is a congenital anomaly resulting from
appearance with a thickened esophageal wall, hypo-inten- abnormal embryological development. The lesion is the
sity on T1WI, and slight high-intensity on T2-weighted second most common benign lesion of the esophagus,
images (T2WI). accounting for 0.5–2.5 % of all esophageal tumors [1].
Approximately 20 % of these lesions communicate with
the esophageal lumen [2].
Benign tumors and conditions Duplication cysts are found in the lower half and on the
right aspect of the esophagus because the foregut epithe-
Leiomyoma lium undergoes dextrorotation [11]. Esophagography shows
a well-defined extrinsic compression and may demonstrate
Leiomyoma is the most common benign tumor of the communication with the lumen. Although T2WI depicts
esophagus, accounting for at least 50 % of such tumors [1]. common features of cysts such as bright hyper-intensity,

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Jpn J Radiol (2016) 34:321–330 325

◂Fig. 6  Esophageal schwannoma in a 52-year-old man. a Barium


esophagography shows the filling defect caused by extrinsic compres-
sion of the upper esophagus. b Coronal contrast-enhanced CT shows
the fusiform mass with heterogeneous enhancements (arrow). c The
mass appears as hyper-intensity on T2WI

CT and T1WI may depict variable attenuation and inten-


sity that depends on the contents, such as hemorrhagic and
mucoid material (Fig. 11).

Fibrovascular polyp

Esophageal fibrovascular polyp is a rare intraluminal tumor


consisting of fibrous, vascular, and adipose tissue. These
lesions represent less than 2 % of all benign esophageal
tumors [2].
The location of esophageal fibrovascular polyp is usu-
ally the cervical esophagus near the cricopharyngeus

Fig. 7  Esophageal granular cell tumor in a 67-year-old man. a Bar-


ium esophagography shows the sessile protrusion with a trapezoid
shape in the middle esophagus (arrow). b Endoscopy reveals the yel-
lowish lesion covered with normal mucosa

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326 Jpn J Radiol (2016) 34:321–330

◂Fig. 8  Esophageal leiomyoma in a 31-year-old man. a Barium


esophagography shows the smooth filling defect with an obtuse
angle in the upper to middle esophagus. b CT shows the homogene-
ous low-attenuation mass with calcification in the right esophagus. c
The horseshoe-shaped mass involving the upper to middle esophagus
appears as a hypo-intensity area on coronal T2WI

Fig. 9  Blue rubber bleb nevus syndrome in a 70-year-old woman.


a, b Upper gastrointestinal series show the protruding lesion in the
lower esophagus and smooth filling defect in the greater curvature of
stomach (arrow)

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Jpn J Radiol (2016) 34:321–330 327

Fig. 10  Esophageal hemangioma in a 42-year-old man. a–c The


mass in the lower esophagus appears as an area of hypo-intensity on
T1WI, hyper-intensity on fat suppression T2WI, and homogeneous
enhancement on fat-suppression T1WI after administration of gado-
linium-containing MRI contrast agents

muscle. Esophagography reveals a smooth and sausage-like


mass with an unclear proximal pedicle. Fat-attenuation on
CT and hyper-intensity on T1WI can be visualized predom- Fig. 11  Duplication cyst in a 47-year-old man. a Barium esophago-
inantly when the amount of adipose tissue is larger in quan- graphy shows extrinsic compression at the lower esophagus. b Con-
trast-enhanced CT shows the well-defined mass with low attenuation
tity than other tissue types (Fig. 12) [2]. at the right of the esophagus (arrow). c T2WI shows the homogene-
ous hyper-intensity mass
Papilloma
irritation from reflux esophagitis or human papilloma virus
Squamous papilloma of the esophagus (SPE) is a rare epi- (HPV) infection [9, 12]. Whether this is a malignant degen-
thelial tumor characterized by a finger-like growth pattern eration of SPE is also not sufficiently clear [12].
covered with fibrovascular cores. The etiology of this tumor SPE arises in the lower third of the esophagus, whereas
remains unclear, but suggested causes include chronic many lesions associated with HPV are found in a proximal

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328 Jpn J Radiol (2016) 34:321–330

Fig. 13  Squamous papilloma in a 47-year-old woman. a Barium


esophagography shows the cauliflower-like lesion in the lower esoph-
agus. b Endoscopy reveals the wart-like reddish protrusion (color fig-
ure online)

Esophageal tuberculosis consists of epithelioid granuloma


with Langhans cells and central necrosis in the submucosa.
Esophageal tuberculosis locates in the middle esopha-
Fig. 12  Esophageal fibrovascular polyp in a 55-year-old woman. gus. Esophagography reveals an ulceration, pseudotumor
a Barium esophagography shows the intraluminal polypoid filling
defect extending to the distal from the proximal esophagus. b Con- with calcification in the submucosa, and tracheoesopha-
trast-enhanced CT shows the well-circumscribed mass with fat den- geal fistula (Fig. 14) [1]. CT demonstrates a thickened wall
sity (arrow) of the esophagus, a mass with central low attenuation and
peripheral enhancement, and lymphadenopathy.

location [9]. On esophagography, the cauliflower-like lesion Candida


of SPE is seen (Fig. 13).
Candida albicans is the most common cause of infectious
Tuberculosis esophagitis and is found in immunocompromised patients,
such as those with acquired immunodeficiency syndrome,
Esophageal tuberculosis is extremely rare, constituting and following chemotherapy and radiotherapy. Infected
approximately 0.2 % of gastrointestinal tuberculosis [13]. achalasia or scleroderma patients are also described.

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Jpn J Radiol (2016) 34:321–330 329

Fig. 14  Old esophageal tuberculosis in a 74-year-old man. Barium Fig. 16  Inlet patch in a 59-year-old man. Barium esophagography
esophagography shows the smooth filling defect with calcification in shows the pair of thin protrusions in the upper esophagus (arrows)
the middle esophagus

advanced stage, irregular or shaggy esophageal walls,


called pseudodiverticulosis, can develop from the mucosa
over weakened muscle layers [14]. CT reveals wall thick-
ening and submucosal edema, which may form the target
signs (Fig. 15).

Inlet patch

Ectopic gastric mucosa in the upper esophagus is a congen-


ital anomaly constituting 10 % of the population who have
undergone endoscopy, called an “inlet patch” [9]. An inlet
patch originates from replacement of squamous epithe-
lium by columnar epithelium during embryonic develop-
ment. Adenocarcinoma in the upper esophagus infrequently
occurs in inlet patch areas.
Inlet patches locate in the upper esophagus, especially
the post-cricoid portion, because squamous epithelium
extends from the middle into the upper and lower esopha-
gus. The characteristic findings of esophagography are the
rim-like protrusion and a pair of indentations (Fig. 16).

Conclusions
Fig. 15  Candida in a 53-year-old man. Barium esophagography
shows the characteristic diffuse plaque-like lesions and intraluminal
Esophageal protruding lesions include a wide spectrum of
pseudodiverticulosis
malignant and benign tumors. The features outlined in this
paper will help radiologists differentiate the various types
Esophagography demonstrates the diffuse plaque-like of lesions that protrude into the esophagus.
filling defects in the early stages of this disease. At a more

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330 Jpn J Radiol (2016) 34:321–330

Compliance with ethical standards  7. Amano M, Okuda T, Amano Y, Tajiri T, Kumazaki T. Magnetic
resonance imaging of gastrointestinal stromal tumor in the abdo-
Conflict of interest  No authors have any conflicts of interest to dis- men and pelvis. Clin Imaging. 2006;30(2):127–31.
close. 8. Yoon HY, Kim CB, Lee YH, Kim HG. An obstructing
large schwannoma in the esophagus. J Gastrointest Surg.
2008;12(4):761–3.
9. Tsai SJ, Lin CC, Chang CW, et al. Benign esophageal lesions:
References endoscopic and pathologic features. World J Gastroenterol.
2015;21(4):1091–8.
1. Noh HM, Fishman EK, Forastiere AA, Bliss DF, Calhoun PS. 10. Kassarjian A, Fishman SJ, Fox VL, Burrows PE. Imaging

CT of the esophagus: spectrum of disease with emphasis on characteristics of blue rubber bleb nevus syndrome. AJR Am J
esophageal carcinoma. Radiographics. 1995;15(5):1113–34. Roentgenol. 2003;181(4):1041–8.
2. Lewis RB, Mehrotra AK, Rodriguez P, Levine MS. 11. Arbona JL, Fazzi JG, Mayoral J. Congenital esophageal cysts:
From the radiologic pathology archives: esophageal neo- case report and review of literature. Am J Gastroenterol.
plasms: radiologic–pathologic correlation. Radiographics. 1984;79(3):177–82.
2013;33(4):1083–108. 12. Mosca S, Manes G, Monaco R, Bellomo PF, Bottino V, Balzano
3. Iascone C, Barreca M. Carcinosarcoma and pseudosarcoma of A. Squamous papilloma of the esophagus: long-term follow up. J
the esophagus: two names, one disease—comprehensive review Gastroenterol Hepatol. 2001;16(8):857–61.
of the literature. World J Surg. 1999;23(2):153–7. 13. Welzel TM, Kawan T, Bohle W, Richter GM, Bosse A, Zoller
4. Yamamoto Y, Watanabe Y, Horiuchi A, et al. True carcinosar- WG. An unusual cause of dysphagia: esophageal tuberculosis. J
coma of the esophagus: report of a case. Case Rep Gastroenterol. Gastrointest Liver Dis. 2010;19(3):321–4.
2008;2(3):330–7. 14. Sam JW, Levine MS, Rubesin SE, Laufer I. The “foamy” esoph-
5. Isiklar I, Leeds NE, Fuller GN, Kumar AJ. Intracranial metastatic agus: a radiographic sign of Candida esophagitis. AJR Am J
melanoma: correlation between MR imaging characteristics and Roentgenol. 2000;174(4):999–1002.
melanin content. AJR Am J Roentgenol. 1995;165(6):1503–12.
6. Mu ZM, Xie YC, Peng XX, et al. Long-term survival after enu-
cleation of a giant esophageal gastrointestinal stromal tumor.
World J Gastroenterol. 2014;20(37):13632–6.

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