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1.
Turk Patoloji Derg ; 32(1): 44-6, 2016.
Article in English | MEDLINE | ID: mdl-26832182

ABSTRACT

PEComas are uncommon mesenchymal tumors often involving the pelvic organs. They have an unpredictable behavior. Accurate diagnosis and long-term follow-up is therefore essential in these patients. We report this case of PEComa of uncertain malignant potential in an unusual location with excellent prognosis.


Subject(s)
Broad Ligament/pathology , Perivascular Epithelioid Cell Neoplasms/pathology , Adult , Biomarkers, Tumor/analysis , Female , Humans , Immunohistochemistry
2.
Indian J Dermatol ; 60(2): 214, 2015.
Article in English | MEDLINE | ID: mdl-25814743

ABSTRACT

Trichofolliculomas are benign hair follicle hamartomas which were initially considered as hair follicle tumors. Usually presenting as a solitary lesion associated with a tuft of vellus hairs, multiple trichofolliculomas are rare. Trichofolliculomas are characterized by a histopathological feature of dermal keratin cyst with cyst wall showing radiating hair follicles. We report this case for the rare presentation of multiple trichofolliculomas on the face which clinically mimicked multiple trichoepitheliomas.

3.
J Clin Diagn Res ; 8(12): FD01-2, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25653958

ABSTRACT

Hepatic epithelioid haemangio-endothelioma (HEHE) is a rare vascular tumour of endothelial origin. The etiology of this tumour is unknown and has a variable clinical outcome. It usually affects adults and is extremely rare in children. Histologically, HEHE is characterized by epithelioid to dendritic tumour cells with intracytoplasmic lumina containing RBCs and a myxoid to sclerotic stroma. Being a rare entity, awareness and a high degree of suspicion is required to correctly identify this tumour. We report a case of hepatic hemangioendothelioma in an 8-year-old child.

4.
Case Rep Nephrol ; 2012: 239093, 2012.
Article in English | MEDLINE | ID: mdl-24533202

ABSTRACT

Botryomycosis is a unique form of bacterial infection, closely mimicking actinomycosis. The usual site of occurrence is the skin and renal botryomycosis is very rare. The most common organism is Staphylococcus aureus which can be identified using Gram stain and confirmed by culture. Early and accurate diagnosis can ensure appropriate antibiotic therapy. We present a young lady diagnosed to have incidental botryomycosis of the kidney, following nephrectomy.

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