3
Can Respir J Vol 15 No 4 May/June 2008 217 Diagnosis of elastofibroma Cuneyt Tetikkurt MD 1 , Seza Tetikkurt MD 2 , Nihal Bayar MD 1 1 Department of Pulmonary Diseases, Cerrahpasa Faculty of Medicine, Istanbul University; 2 Department of Pathology, Taksim Training and Research Hospital, Istanbul, Turkey Correspondence: Dr Cuneyt Tetikkurt, Tanzimat Sok Serkan Apartment 8/16, Caddebostan 34827, Istanbul, Turkey. Telephone 212-414-32-17 or 216-360-19-77, fax 216-414-32-17, e-mail [email protected] C Tetikkurt, S Tetikkurt, N Bayar. Diagnosis of elastofibroma. Can Respir J 2008;15(4):217-218. Elastofibroma is a relatively rare soft tissue mass. The lesion is proba- bly reactive and occurs most commonly in the periscapular region. It is a degenerative benign neoplasm with the clinical appearence of a malignant tumour. The present report describes the case of a 70-year- old man with bilateral elastofibroma. The diagnosis was established with needle aspiration biopsy and positron emission tomography/computed tomography. The present case suggests that needle aspiration biopsy and positron emission tomography/computed tomography are highly useful in the diagnosis of this rare, benign tumour. Key Words: Elastofibroma; Mesenchymal tumours; Needle aspiration biopsy; PET/CT Un diagnostic d’élastofibrome L’élastofibrome est une masse relativement rare des tissus mous. Selon toute probabilité, la lésion est réactive et elle se produit surtout dans la région périscapulaire. C’est un néoplasme bénin évolutif à l’apparence clinique d’une tumeur maligne. Le présent rapport décrit le cas d’un homme de 70 ans atteint d’un élastofibrome bilatéral. Le diagnostic a été posé au moyen d’une aspiration à l’aiguille, d’une tomographie par émis- sion de positrons et d’une tomodensitométrie. Le présent cas laisse sup- poser que l’aspiration à l’aiguille, la tomographie par émission de positrons et la tomodensitométrie sont hautement utiles pour diagnostiquer cette tumeur bénigne rare. E lastofibroma is a rare, slow growing, ill-defined soft tissue tumour of the chest wall. It is commonly located beneath the rhomboid major and latissimus dorsi muscles. The tumour is usually unilateral (1). Recognition of the lesion is important because the differential diagnosis includes malignant tumours. We report a case of bilateral elastofibroma, in which needle aspiration biopsy and positron emission tomography/computed tomography (PET/CT) permitted the diagnosis of this rare, benign tumour, eliminating the need for preoperative histolog- ical examination. CASE PRESENTATION A 70-year-old male dentist presented with two painful masses located bilaterally in the right and left inferior periscapular region. The masses had enlarged slowly over the previous 12 months. The pain increased in intensity and radiated back bilaterally. The patient’s medical and family history did not reveal any diseases. The patient did not smoke or use any drugs. Physical examination revealed a tender, firm mass with a diameter of 70 mm in the left infrascapular region, and a ten- der, firm mass with a diameter of 50 mm in the right infra- scapular region. No associated lymphadenopathy was found. Initial investigations showed a normal blood count, bone pro- file, inflammatory markers and a normal chest radiograph. CT of the chest revealed two well-defined soft tissue lesions, with a striated appearance, measuring 70 mm × 20 mm on the left inferior scapular region and 50 mm × 15 mm on the right infe- rior scapular region. A needle aspiration biopsy was performed on both sides. The smear was characterized by a mixture of uniform spindle cells and very few mature adipocytes, with fragments of collagen bundles and fibres. PET/CT images showed poorly circumscribed, bilateral soft tissue masses between the inferior tips of the scapulae and chest wall, with low-grade, diffuse 18 F fluorodeoxyglucose uptake (Figure 1). Bilateral surgical excision of the lesions was performed. Postoperative histopathological examination of the resected tumours revealed scant fibroelastic proliferation, with abun- dant hyalinized collagen and entrapped mature adipose tissue, consistent with the diagnosis of elastofibroma. The patient was asymptomatic after surgery, with no recurrence of the masses. ©2008 Pulsus Group Inc. All rights reserved CASE REPORT Figure 1) Positron emission tomography/computed tomography reveal- ing low, diffuse 18 F fluorodeoxyglucose uptake on both sides

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Page 1: Diagnosis of elastofibroma - Hindawi Publishing Corporationdownloads.hindawi.com/journals/crj/2008/638624.pdfDiagnosis of elastofibroma. Can Respir J 2008;15(4):217-218. Elastofibroma

Can Respir J Vol 15 No 4 May/June 2008 217

Diagnosis of elastofibroma

Cuneyt Tetikkurt MD1, Seza Tetikkurt MD2, Nihal Bayar MD1

1Department of Pulmonary Diseases, Cerrahpasa Faculty of Medicine, Istanbul University; 2Department of Pathology, Taksim Training andResearch Hospital, Istanbul, Turkey

Correspondence: Dr Cuneyt Tetikkurt, Tanzimat Sok Serkan Apartment 8/16, Caddebostan 34827, Istanbul, Turkey. Telephone 212-414-32-17or 216-360-19-77, fax 216-414-32-17, e-mail [email protected]

C Tetikkurt, S Tetikkurt, N Bayar. Diagnosis of elastofibroma.

Can Respir J 2008;15(4):217-218.

Elastofibroma is a relatively rare soft tissue mass. The lesion is proba-

bly reactive and occurs most commonly in the periscapular region. It

is a degenerative benign neoplasm with the clinical appearence of a

malignant tumour. The present report describes the case of a 70-year-

old man with bilateral elastofibroma. The diagnosis was established

with needle aspiration biopsy and positron emission

tomography/computed tomography. The present case suggests that

needle aspiration biopsy and positron emission tomography/computed

tomography are highly useful in the diagnosis of this rare, benign

tumour.

Key Words: Elastofibroma; Mesenchymal tumours; Needle

aspiration biopsy; PET/CT

Un diagnostic d’élastofibrome

L’élastofibrome est une masse relativement rare des tissus mous. Selon

toute probabilité, la lésion est réactive et elle se produit surtout dans la

région périscapulaire. C’est un néoplasme bénin évolutif à l’apparence

clinique d’une tumeur maligne. Le présent rapport décrit le cas d’un

homme de 70 ans atteint d’un élastofibrome bilatéral. Le diagnostic a été

posé au moyen d’une aspiration à l’aiguille, d’une tomographie par émis-

sion de positrons et d’une tomodensitométrie. Le présent cas laisse sup-

poser que l’aspiration à l’aiguille, la tomographie par émission de positrons

et la tomodensitométrie sont hautement utiles pour diagnostiquer cette

tumeur bénigne rare.

Elastofibroma is a rare, slow growing, ill-defined soft tissuetumour of the chest wall. It is commonly located beneath

the rhomboid major and latissimus dorsi muscles. The tumouris usually unilateral (1). Recognition of the lesion is importantbecause the differential diagnosis includes malignant tumours.We report a case of bilateral elastofibroma, in which needleaspiration biopsy and positron emission tomography/computedtomography (PET/CT) permitted the diagnosis of this rare,benign tumour, eliminating the need for preoperative histolog-ical examination.

CASE PRESENTATIONA 70-year-old male dentist presented with two painful masseslocated bilaterally in the right and left inferior periscapularregion. The masses had enlarged slowly over the previous12 months. The pain increased in intensity and radiated backbilaterally. The patient’s medical and family history did notreveal any diseases. The patient did not smoke or use anydrugs. Physical examination revealed a tender, firm mass witha diameter of 70 mm in the left infrascapular region, and a ten-der, firm mass with a diameter of 50 mm in the right infra-scapular region. No associated lymphadenopathy was found.Initial investigations showed a normal blood count, bone pro-file, inflammatory markers and a normal chest radiograph. CTof the chest revealed two well-defined soft tissue lesions, witha striated appearance, measuring 70 mm × 20 mm on the leftinferior scapular region and 50 mm × 15 mm on the right infe-rior scapular region. A needle aspiration biopsy was performedon both sides. The smear was characterized by a mixture ofuniform spindle cells and very few mature adipocytes, with

fragments of collagen bundles and fibres. PET/CT imagesshowed poorly circumscribed, bilateral soft tissue massesbetween the inferior tips of the scapulae and chest wall, withlow-grade, diffuse 18F fluorodeoxyglucose uptake (Figure 1).Bilateral surgical excision of the lesions was performed.Postoperative histopathological examination of the resectedtumours revealed scant fibroelastic proliferation, with abun-dant hyalinized collagen and entrapped mature adipose tissue,consistent with the diagnosis of elastofibroma. The patient wasasymptomatic after surgery, with no recurrence of the masses.

©2008 Pulsus Group Inc. All rights reserved

CASE REPORT

Figure 1) Positron emission tomography/computed tomography reveal-ing low, diffuse 18F fluorodeoxyglucose uptake on both sides

10524_tetikkurt.qxd 28/05/2008 11:40 AM Page 217

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DISCUSSIONElastofibroma, first described in 1961, is a benign, slow-growingmesenchymal soft tissue lesion (2,3). An incidental prevalenceof 2% was found in an elderly population examined using chestCT, but an autopsy series found a frequency of 11.2% in menand 24.4% in women (4,5). The characteristic location isbetween the chest wall and the inferior tip of the scapula.Bilateral involvement occurs in only 10% of patients (6). Thecause and pathogenesis are unclear, but it is believed that sub-clinical microtrauma may lead to reactive hyperplasia of elasticfibres, with a consequent increase in the production of fibroustissue (7). Most patients are asymptomatic, but may presentwith a painless swelling – less than 10% of patients have pain(8). Plain radiographs may be normal or may show soft tissuedensity in the periscapular region. CT usually shows a het-erogenous soft tissue mass with poorly defined margins (9).

Magnetic resonance imaging is the most useful diagnostic tool(10). The differential diagnosis includes desmoid tumours, neu-rofibroma and liposarcoma. Biopsy should, therefore, be under-taken as the confirmatory procedure, and to exclude sarcoma.

Recently, two cases of elastofibroma, in which PET/CT wasused incidentally, were reported (11,12). PET/CT revealed lowto moderate metabolic activity in these patients. In the presentcase, needle aspiration cytology and low-grade diffuse 18F fluo-rodeoxyglucose uptake during PET/CT strongly suggestedelastofibroma.

We believe that needle aspiration biopsy and PET/CT areuseful, noninvasive procedures for the identification ofelastofibroma. Recognition of this low, diffuse metabolic activ-ity with consistent needle aspiration cytology will prevent theuse of unnecessary medical, radiological or surgical interven-tions to establish the diagnosis.

Tetikkurt et al

Can Respir J Vol 15 No 4 May/June 2008218

REFERENCES1. Kara M, Dikmen E, Kara SA, Atasoy P. Bilateral elastofibroma

dorsi: Proper positioning for an accurate diagnosis. Eur J Cardiothorac Surg 2002;22:839-41.

2. Järvi OH, Saxen AE. Elastofibroma dorsi. Acta Pathol MicrobiolScand 1961;144(Suppl 51):83-4.

3. Giebel GD, Bierhoff E, Vogel J. Elastofibroma and pre-elastofibroma – a biopsy and autopsy study. Eur J Surg Oncol1996;22:93-6.

4. Brandser EA, Goree JC, El-Khoury GY. Elastofibroma dorsi:Prevalence in an elderly patient population as revealed by CT. AJR Am J Roentgenol 1998;171:977-80.

5. Järvi OH, Länsimies PH. Subclinical elastofibromas in the scapularregion in an autopsy series. Acta Pathol Microbiol Scand [A]1975;83:87-108.

6. Kransdorf MJ, Meis JM, Montgomery E. Elastofibroma: MR and CT appearance with radiologic-pathologic correlation.AJR Am J Roentgenol 1992;159:575-9.

7. Machens HG, Mechtersheimer R, Göhring U, Schlag PN. Bilateral elastofibroma dorsi. Ann Thorac Surg 1992;54:774-6.

8. Greenberg JA, Lockwood RC. Elastofibroma dorsi: A case reportand review of the literature. Orthop Rev 1989;18:329-33.

9. Hoffman JK, Klein MH, McInerney VK. Bilateral elastofibroma: A case report and review of the literature. Clin Orthop Relat Res1996:245-50.

10. Domanski HA, Carlén B, Sloth M, Rydholm A. Elastofibroma dorsihas distinct cytomorphologic features, making diagnostic surgicalbiopsy unnecessary: Cytomorphologic study with clinical,radiologic, and electron microscopic correlations. Diagn Cytopathol 2003;29:327-33.

11. Patrikeos A, Breidahl W, Robins P. F-18 FDG uptake associatedwith Elastofibroma dorsi. Clin Nucl Med 2005;30:617-8.

12. Wasyliw CW, Caride VJ. Incidental detection of bilateralelastofibroma dorsi with F-18 FDG PET/CT. Clin Nucl Med2005;30:700-1.

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