• Sonuç bulunamadı

A rare benign tumor mimicking malignancy

N/A
N/A
Protected

Academic year: 2021

Share "A rare benign tumor mimicking malignancy"

Copied!
2
0
0

Yükleniyor.... (view fulltext now)

Tam metin

(1)

298

A 75-year-old man with intermittent dry cough and progressive dyspnea on exertion was admitted to our clinic. He had a past history of coronary artery dise- ase and a coronary artery bypass grafting operation.

He had a 20 pack-year history of smoking.

The admission chest X-ray revealed consolidation and atelectasis at basal part of the right lung (Figure 1).

Chest computed tomography (CT) demostrated ple- ural thickening, pleural effusion, and middle lobe late- ral segment atelectasis of the right side suggesting bronchial obstruction (Figure 2).

The patient underwent fiberoptic bronchoscopy which showed an endobronchial polypoid lesion without a pe- duncle originating from the orifice of the lateral seg- ment of the middle lobe (Figure 3). Mucosa of the lesi- on was shiny, thin, reddish, and had a rich vascularisa- tion, mimicing a malignant tumor. Bronchoscopic re- section was not considered feasible because it was im- possible to clearly identify the tumor's endobronchial origin. Bronchial mucosal biopsy was not performed because of risk of hemorrhage. Bronchial lavage was performed from the lateral segment of the middle lobe.

A rare benign tumor mimicking malignancy

Fatma ÇİFTÇİ1, Murat ÖZKAN2, Murat ŞAHİN2, Gökhan KOCAMAN2, Aydın ÇİLEDAĞ1, Akın KAYA1, Hakan KUTLAY2

1 Ankara Üniversitesi Tıp Fakültesi, Göğüs Hastalıkları Anabilim Dalı, Ankara.

2 Ankara Üniversitesi Tıp Fakültesi, Göğüs Cerrahisi Anabilim Dalı, Ankara.

Yazışma Adresi (Address for Correspondence):

Dr. Fatma ÇİFTÇİ, Ankara Üniversitesi Tıp Fakültesi, Göğüs Hastalıkları Anabilim Dalı, Cebeci, ANKARA - TURKEY

e-mail: fatmarslann@yahoo.com

EDİTÖRE MEKTUP/LETTER TO THE EDITOR

Tuberk Toraks 2012; 60(3): 298-299 Geliş Tarihi/Received: 24/07/2012 - Kabul Ediliş Tarihi/Accepted: 31/07/2012

Figure 1. Chest X-ray of the patient. Figure 2. Computed tomography of the chest.

(2)

Patient underwent surgery with right thoracotomy. At bronchotomy, a yellow smooth fatty lesion occluding the middle bronchus was found, frozen section of which yielded no neoplastic tissue. Wedge shape bronchotomy was performed and the lesion was re- sected with its base (Figure 4).

Histopathological diagnosis was endobronchial lipo- ma that had a higher number of mature lymphocytes than other cellular components.

Endobronchial lipoma is an extremely rare benign en- dobronchial tumor. In 1979 Schraufnagel et al. repor- ted a benign tumor prevalance of 3% while endob- ronchial lipoma prevalence of only 0.1% (1). Diagno- sis of the tumor is often obtained by bronchoscopic bi- opsy; however, sometimes it can only be put by bronchotomy or thoracotomy, as in this case (2-4).

Bronchoscopic resection should be considered the first choice of treatment for bronchial lipoma; nevert- heless, surgical resection is reserved for some pati- ents. Surgical resection is preferred when there is dif- ficulty in definite diagnosis and there is a possibility of a complicated malignant tumor (5-7).

CONFLICT of INTEREST None declared.

REFERENCES

1. Schraufnagel DE, Morin JE, Wang NS. Endobronchial lipo- ma. Chest 1979; 75: 1979.

2. Simmers TA, Jie C, Sie B. Endobronchial lipoma posing as carcinoma. Neth J Med 1997; 51: 143-5.

3. Suzuki N, Takizawa H, Yamaguchi M, Matsuzaki G, Kiyosawa H, Dohi M, et al. A case of asymptomatic endob- ronchial lipoma followed for 4 years. Jpn J Thorac Dis 1992;

30: 1879-83.

4. Celik G, Kaya A, Ozdemir O, Ozdemir N, Dizbay Sak S, Al- per D. Endobronchial lipoma: a case report. Tuberk Toraks 2003; 51: 432-5.

5. Destito C, Romagnoli A, Carlucci I, Mercuri M, Vulpio C, Wiel Marin A. Endobronchial lipoma: endoscopic resection or sur- gical excision? Report of a case and review of the literature.

G Chir 1995; 16: 445-7.

6. Muraoka M, Akamine S, Nagayasu T, Iseki M, Suyamo N, Ayabe H. Endobronchial lipoma: review of 64 cases reported in Japan. Chest 2003; 123: 293-6.

7. Yokozaki M, Kodama T, Yokose T, Nishimura M, Yoshida J, Mizokami H, et al. Endobronchial lipoma: a report of three cases. Jpn J Clin Oncol 1996; 26: 53-5.

Çiftçi F, Özkan M, Şahin M, Kocaman G, Çiledağ A, Kaya A, Kutlay H.

299

Tuberk Toraks 2012; 60(3): 298-299 Figure 3. Bronchoscopic imaging of the lesion.

Figure 4. Macroscopic appearence of the resected lesion.

Referanslar

Benzer Belgeler

Chest computed tomography (CT) (Figure 1a and b) revealed nodular formations surrounded by ground-glass opacities in the right anterior upper lobe, right middle lobe,

Familial Mediterranean Fever is a Rare Cause of Recurrent Pleural Effusion.. Tekrarlayan Plevral Efüzyonun Nadir Bir Nedeni Ailevi

Ninety- eight percent of the patients can be diagnosed and treated at an early stage based on typical chest pain, presence of risk factors, dynamic ECG changes and el-

ABSTRACT Objective: The aim of this study was to evaluate the role of diffusion-weighted magnetic resonance imaging (dMRI) in dif- ferentiating between diffuse malignant and

Sonuç olarak; hepatit A ilişkili plevral efüzyonun kesin mekanizması tam bilinmemesine rağmen; karaciğer enfla- masyonun bağlı, immün kompleklere bağlı, asite sekonder veya

"Small bowel feces sign” (arrow) at the level of transition point in the lumen of the small bowel is observed in an axial contrast- enhanced CT image of the 55-year-old

This re- port focuses on a 69-year-old female patient diagnosed with relapsed CLL who developed grade 4 TLS after ibrutinib monotherapy.. The patient developed TLS on the third day

Splenic hamartoma, which is one of the primary benign tumors of the spleen, is usually asymptomatic and is typically detected incidentally on imaging.. It is also difficult to