Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
1.
Indian J Pathol Microbiol ; 63(1): 106-108, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32031135

RESUMEN

Monotypic angiomyolipoma is usually found in the kidneys and is composed predominantly of epithelioid cells which show positivity for melanocyte and smooth muscle markers. It can pose a diagnostic challenge due to a range of differential diagnosis. We report the second case of monotypic angiomyolipoma of nasal cavity and first from India in a 54-year-old male who presented with a nasal polyp. Grossly the tumor was well circumscribed and un-encapsulated. Microscopy showed a large number of epithelioid cells mixed with a few spindle cells, varying sized blood vessels, and focal areas of adipose tissue. Immunohistochemistry was positive for smooth muscle actin (SMA) and human melanoma black (HMB-45) stains. It is important to identify this tumor as it can sometimes be mistaken for malignancy and only needs endoscopic resection.


Asunto(s)
Angiomiolipoma/diagnóstico por imagen , Epistaxis/etiología , Cavidad Nasal/patología , Neoplasias Nasales/diagnóstico por imagen , Biomarcadores de Tumor , Diagnóstico Diferencial , Técnicas Histológicas , Humanos , Inmunohistoquímica , Masculino , Persona de Mediana Edad , Cavidad Nasal/diagnóstico por imagen , Pólipos Nasales/patología , Neoplasias Nasales/cirugía , Tomografía Computarizada por Rayos X
2.
Indian J Pathol Microbiol ; 61(3): 437-439, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30004076

RESUMEN

Spermatocytic seminoma (SCS) is an indolent germ cell tumor of the testis. It has an excellent prognosis and orchidectomy is generally curative. Very rarely, it can be complicated by a sarcomatous transformation which is associated with a very aggressive behavior and requires adjuvant therapy. SCS with sarcomatous component is a very rare occurrence with <20 cases described in the world literature of which eight showed rhabdomyoblastic differentiation. We report a case of SCS with rhabdomyosarcomatous differentiation in a 60-year-old male along with a short review of literature.


Asunto(s)
Diferenciación Celular , Rabdomiosarcoma/diagnóstico , Seminoma/diagnóstico , Neoplasias Testiculares/diagnóstico , Testículo/patología , Humanos , Masculino , Persona de Mediana Edad , Orquiectomía , Pronóstico , Rabdomiosarcoma/patología , Rabdomiosarcoma/ultraestructura , Seminoma/patología , Neoplasias Testiculares/patología , Testículo/citología , Testículo/diagnóstico por imagen , Ultrasonografía
3.
J Midlife Health ; 9(1): 44-46, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29628730

RESUMEN

Pure squamous cell carcinoma (SCC) of the ovary is rare. SCC can arise in a mature teratoma (MT), ovarian endometriosis or in a Brenner tumor. SCC is the most common malignant transformation arising in MT and comprises 80% of all cases. Such neoplastic transformations are extremely difficult either to predict or detect early. The mechanism of malignant transformation has not been completely understood. Due to the rarity and the aggressive course, diagnosis and treatment constitute a big challenge. We report a case of SCC arising in MT presenting with a huge abdominopelvic mass and abundant peritoneal collections clinically masquerading as abdominal tuberculosis. A review of literature with special emphasis on prognosis and treatment modalities is also presented.

4.
J Clin Diagn Res ; 11(2): ED10-ED11, 2017 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-28384874

RESUMEN

Spindle Cell Lipoma (SCL) is an uncommon benign tumour of adipose tissue that is usually superficially located in the neck, back and shoulder region. Although it has characteristic histological features it can pose a diagnostic dilemma on cytology. It presents with a mixture of spindle cells, adipocytes, collagen fibres and a myxoid matrix in varying proportions sometimes with mild pleomorphism. Hence, it can be mistaken for other spindle cell, adipose and myxoid tumours which can be benign or malignant. We present a case of SCL of the back in a 47-year-old male, who presented with a slow growing lesion. Fine Needle Aspiration Cytology (FNAC) showed the characteristic cytological features described above and a diagnosis could be given after clinical correlation. We report this case as the cytology of this uncommon tumour has been described in relatively few cases and a correct pre-operative diagnosis will aid in proper management of this tumour.

6.
Indian J Pathol Microbiol ; 54(1): 47-50, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21393876

RESUMEN

CONTEXT: To identify various causes, risk factors, age and sex distribution associated with sudden and unexpected natural deaths (SUNDs) in young adults of age between 18 and 35 years. MATERIALS AND METHODS: Retrospective analysis of autopsy reports and medical records of all SUNDs that occurred instantaneously or within 24 hours of onset of symptoms in young adults, between 2001 and 2009. RESULT: Of the total 6453 deaths autopsied during 2001-2009, 64 (0.99%) were SUNDs in young adults, chiefly in males between 30 and 35 years of age. Non-cardiac causes significantly predominated (73.4%) over cardiac causes (7.8%). Most of the SUND cases were due to preventable causes, including infections (54.6% cases), cerebrovascular accidents (9.37%) and ischemic cardiac causes (6.25%). Sudden adult death syndrome (SADS) accounted for 18.75% deaths. CONCLUSION: SUND in young adults is preventable. A meticulous post-mortem examination with special attention to the conduction system of heart and detailed toxicological analysis can pinpoint the cause of death in SADS.


Asunto(s)
Muerte Súbita/epidemiología , Muerte Súbita/etiología , Adolescente , Adulto , Autopsia , Enfermedades Transmisibles/mortalidad , Femenino , Humanos , Masculino , Isquemia Miocárdica/mortalidad , Prevalencia , Estudios Retrospectivos , Accidente Cerebrovascular/mortalidad , Adulto Joven
SELECCIÓN DE REFERENCIAS
Detalles de la búsqueda