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1.
Rom J Morphol Embryol ; 63(1): 221-228, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36074688

RESUMO

Basaloid squamous cell carcinoma (BSCC) is an aggressive type of squamous cell carcinoma (SCC) predominant in the upper aerodigestive tract. To our knowledge, only one case of that tumor has been previously described in the parotid gland. Shadow (ghost) cell differentiation (SCD) is a specialized form of keratinization characteristic of pilomatricoma, and other skin tumors with follicular differentiation. SCD has also been described infrequently in some visceral carcinomas and rarely in the minor salivary glands. Recently, an SCC with prominent SCD has been reported in the parotid. We report for the first time the case of parotid BSCC with prominent SCD in an 87-year-old man. He was admitted due to the appearance in the last few months of a mass, painful on palpation, in the left parotid region. Imaging studies and tru-cut biopsies indicated the need for surgical removal. A left superficial parotidectomy, including the branch of the cervicofacial nerve, was performed. The BSCC showed predominance (62%) of SCD. Immunohistochemically, the basaloid cells were positive for ß-catenin, pan-cytokeratin (pan-CK) AE1∕AE3, CK19, high-molecular-weight CK (HMWCK), p63, p40, and cluster of differentiation 10 (CD10) in a diffuse pattern. No signs of recurrence or metastasis were observed four months after surgery. The main differential diagnoses include nuclear protein in testis (NUT) carcinoma, adamantinoma-like Ewing sarcoma, embryonal carcinoma, and basal cell adenocarcinoma of the solid type. SCD in BSCC of the parotid should be recognized to avoid misdiagnosis, especially in small samples. Although rare, BSCC with SCD should be added to the list of tumors that may originate in the parotid gland.


Assuntos
Adenocarcinoma , Carcinoma de Células Escamosas , Neoplasias das Glândulas Salivares , Adenocarcinoma/patologia , Idoso de 80 Anos ou mais , Carcinoma de Células Escamosas/diagnóstico , Carcinoma de Células Escamosas/patologia , Diferenciação Celular , Humanos , Masculino , Glândula Parótida/patologia , Neoplasias das Glândulas Salivares/patologia
3.
Turk Patoloji Derg ; 31(1): 64-7, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25371024

RESUMO

Conventional lipoma is the most common benign mesenchymal neoplasm in adults. However, bladder lipoma is a rare tumor. We report an incidental 0.5-cm, mucosal, bladder lipoma in a 75-year-old man, successfully treated with endoscopic excision. The tumor was found during the extension study of a high-grade urothelial carcinoma of the renal pelvis. A review of the published cases, including the present report, yielded a total of 16. Conclusions on this review are presented. The case is being reported because its rarity and to highlight the importance of complete workup to clarify associated disorders that may suggest extension of a malignant process.


Assuntos
Achados Incidentais , Neoplasias Renais/patologia , Lipoma/patologia , Neoplasias Primárias Múltiplas/patologia , Neoplasias da Bexiga Urinária/patologia , Idoso , Biópsia , Cistectomia/métodos , Cistoscopia , Humanos , Neoplasias Renais/cirurgia , Lipoma/cirurgia , Masculino , Neoplasias Primárias Múltiplas/cirurgia , Nefrectomia , Valor Preditivo dos Testes , Tomografia Computadorizada por Raios X , Resultado do Tratamento , Neoplasias da Bexiga Urinária/cirurgia
4.
Case Rep Urol ; 2014: 296908, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25184072

RESUMO

Urinary tract endometriosis and endocervicosis are an uncommon pathologic finding, with a common embryological origin. We present 2 cases of female patients with bladder mass. The first one was a finding of a nodular formation in the bladder during study of a nonviable foetus and the second was an incidental finding of a neoformation in the fundus of the bladder during the realization of an ultrasound. In both cases, we performed a surgical management with transurethral resection. Histopathological examination revealed a bladder endometrioma in the first case and endocervicosis with associated endometriosis in the second.

5.
Pathol Res Pract ; 208(1): 62-4, 2012 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-22177594

RESUMO

Xanthogranulomatous orchitis (XGO) is a rare chronic inflammatory process characterized by destruction of tissue that is replaced by an outstanding cellular infiltrate of lipid-laden macrophages. To date, 20 cases of this process have been reported previously. We present herein the case of a 55-year-old man who had sustained complete tetraplegia at C-6 level and neuropathic bladder for 21 years. After repeated episodes of urinary tract infection, the patient developed a bilateral XGO and a right xanthogranulomatous epididymitis (XGE) that were treated with bilateral orchiepididymectomy. To our knowledge, a bilateral XGO has not yet been reported. Repeated episodes of high-pressure urinary reflux along the vas deferens during dyssynergic voiding possibly led to retrograde extension from the urinary tract by common urinary pathogens and development of bilateral XGO and right XGE. Since tissue destruction is a feature of this process, curative treatment required antibiotic therapy followed by bilateral excision of testes and epididymes.


Assuntos
Granuloma/patologia , Orquite/patologia , Quadriplegia/complicações , Xantomatose/patologia , Granuloma/etiologia , Humanos , Masculino , Pessoa de Meia-Idade , Orquite/etiologia , Bexiga Urinaria Neurogênica/complicações , Xantomatose/etiologia
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