Glomus tumour of the trachea: report of a case with microscopic, ultrastructural and immunohistochemical examination and review of the literature

1991 ◽  
Vol 19 (5) ◽  
pp. 459-464 ◽  
Author(s):  
M.D. GARCÍA-PRATS ◽  
M.T. SOTELO-RODRÍGUEZ ◽  
C. BALLESTÍN ◽  
M.A. MARTÍNEZ-GONZÁLEZ ◽  
R. ROCA ◽  
...  
1992 ◽  
Vol 79 (4) ◽  
pp. 345-347 ◽  
Author(s):  
S. D. Heys ◽  
J. Brittenden ◽  
P. Atkinson ◽  
O. Eremin

1992 ◽  
Vol 30 (6) ◽  
pp. 398-400 ◽  
Author(s):  
J.M. Geraghty ◽  
R.W.N. Thomas ◽  
J.M. Robertson ◽  
J.W. Blundell

2020 ◽  
Vol 2 (1) ◽  
pp. 17-23
Author(s):  
M. Darouichi

Glandular-cystic bladder cystitis is a rare, benign non-tumor condition, preferentially located on the area of the bladder trigone and can simulate a malignant tumor. It is a benign reactive metaplasia of the bladder submucosa, characterized by hyperplasia of the islets of Von Brunn and cystic. It is classified among reactive epithelial anomalies of the urothelium, such as islet hyperplasia of Von Brünn, cystitis, glandular cystitis, nephrogenic metaplasia and epidermoid metaplasia. It presents a clinical diagnostic challenge having the expression of a simple recurrent cystitis and misleading the radiological diagnosis evoking a malignant tumor of the bladder. Its certainty diagnosis is histological. We report the case of a 38-year-old young man who consulted for recurrent cystitis. The CT scan showed a vegetative tissue structure of the middle and left medial vesical floor, sawtooth 3 cm long axis suspecting a tumor of the bladder. The patient underwent transurethral resection of the bladder lesion. The histological and immunohistochemical examination concluded with glandular and cystic cystitis (minor form). In the light of this observation, we will discuss the diagnostic difficulties, the pathophysiological mechanisms, the radiological aspects, the anatomopathological, therapeutic features and the prognosis of this rare condition. The literature regarding this entity has been reviewed and the differential diagnosis was discussed.


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Rashna Meunier ◽  
Gyan Pareek ◽  
Ali Amin

Aims. Metastatic malignant melanoma of the urinary bladder is a rare clinical entity, with only twenty-three published cases to date. We present a case of this rare entity, a thorough review of the literature, and differential diagnosis of melanoma in the bladder.Methods and Results. A 55-year-old woman with a history of malignant melanoma of the right thigh, excised eight years ago, presented with back pain, fatigue, and hematuria. She underwent computed tomography (CT) scan and was found to have metastases within the liver, spleen, lungs, and urinary bladder. She underwent cystoscopy and transurethral resection of three polypoid lesions. Histologic and immunohistochemical examination revealed metastatic malignant melanoma involving bladder mucosa.Conclusions. This case illustrates the importance of including malignant melanoma in the differential diagnosis of high grade neoplasms of bladder, especially in cases where the relevant clinical history is not available.


2016 ◽  
Vol 88 (6) ◽  
pp. 653-654 ◽  
Author(s):  
Elan Novis ◽  
Avi Raman ◽  
Fiona Maclean ◽  
Enzo Lazzaro

2014 ◽  
Vol 7 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Tihomir P. Totev ◽  
Svetlana A. Mateva ◽  
Margarita R. Nikolova ◽  
Grigor A. Gorchev

Abstract Angiomyolipomas are benign mesenchymal neoplasms, presenting with a variable mixture of adipose tissue, smooth muscle and vascular component. Although they are typically found in the kidneys, many cases of extrarenal angiomyolipomas have been reported. They are extremely rarely present in the uterus. We describe a case of a 56-year-old woman, operated on for leiomyoma. Total laparohysterectomy and bilateral adnexectomy was performed. After histological and immunohistochemical examination, the final diagnosis of uterine angiomyolipoma was made. Renal and extrarenal angiomyolipomas are compared in regard to clinical and morphological aspect and their difference from PEComas is dicussed. PEComas have been defined during the last decade and there are still issues regarding terminological clarity and overlapping.


Pathology ◽  
2017 ◽  
Vol 49 ◽  
pp. S123-S124
Author(s):  
Y. Sun ◽  
W. Jones ◽  
W. Varikatt ◽  
R. Chin

1995 ◽  
Vol 20 (3) ◽  
pp. 409-412 ◽  
Author(s):  
T. R. TAKEI ◽  
E. A. NALEBUFF

We report a case of an extradigital glomus tumour found in the forearm. A review of the literature suggests that extradigital glomus lesions in the upper limb may be more common than they are thought to be.


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