Results 191 to 200 of about 9,571 (225)

What Is Your Diagnosis? Dermal Mass From the Left Forelimb of a Dog

Veterinary Clinical Pathology, EarlyView.
Heather D. McDavid, Miranda D. Vieson, Robert Armentano, Nicholas T. Noto   +3 more
wiley   +1 more source

Oncocytoma of Palate: A Case Report, with an Emphasis on Immunohistochemistry. [PDF]

J Dent (Shiraz)
Mani S, Mani A, Tripathi VP, Bajpai M, Karakalla SR.   +4 more
europepmc   +1 more source

Immunohistochemical expression of ΔNp63 versus pan-p63 in normal and neoplastic feline tissues. [PDF]

Vet Pathol
Santos IR, Brunner CB, Paz MC, Hartmann G, Tres GZ, Sonne L, Panziera W, Driemeier D, Bandinelli MB, Pavarini SP.   +9 more
europepmc   +1 more source

My Journey into the World of Salivary Gland Sebaceous Neoplasms [PDF]

Head and Neck Pathology, 2012
As part of this symposium honoring Leon Barnes, the authors were asked to present the case from which they learned the most. I chose a cystic sebaceous lymphadenoma (SL) as my case presentation. This paper presents this unusual case, as well as several additional sebaceous tumors that came across my desk the first few years I was in practice.
Douglas R Gnepp, Gnepp Douglas R
exaly   +3 more sources

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Topics in histopathology of sweat gland and sebaceous neoplasms

Journal of Dermatology, 2017
AbstractThis article reviews several topics regarding sweat gland and sebaceous neoplasms. First, the clinicopathological characteristics of poroid neoplasms are summarized. It was recently reported that one‐fourth of poroid neoplasms are composite tumors and one‐fourth are apocrine type lesions.

exaly   +3 more sources

Sebaceous neoplasms of salivary gland origin. Report of 21 cases [PDF]

Cancer, 1984
Primary sebaceous tumors of salivary glands are extremely rare, although sebaceous glands are commonly present in parotid and submandibular glands. A review of the files of the Armed Forces Institute of Pathology yielded 21 cases of primary salivary gland sebaceous tumors.
D R Gnepp
exaly   +3 more sources

All patients with sebaceous gland neoplasms should be screened for Muir-Torre syndrome

Clinical and Experimental Dermatology, 2009
John R Ingram
exaly   +2 more sources

Diagnostic Accuracy of Immunohistochemistry Testing on Sebaceous Gland Neoplasms for Muir‐Torre Syndrome: A Meta‐Analysis

Journal of Cutaneous Pathology
ABSTRACT Background Muir‐Torre syndrome (MTS) is a hereditary tumor predisposition syndrome associated with sebaceous neoplasms. Immunohistochemistry (IHC) for loss of mismatch repair (MMR) proteins in these tumors is used as a screening test, but its diagnostic accuracy has not been rigorously
Garth Fraga
exaly   +3 more sources

Preferential expression of OVOL1 in inner root sheath of hair, sebaceous gland, eccrine duct and their neoplasms in human skin.

Fukuoka igaku zasshi = Hukuoka acta medica, 2014
OVOL1 is an important transcription factor for epidermal keratinization, which suppresses proliferation and switches on the differentiation of keratinocytes. A recent genome-wide association study has revealed that OVOL1 is one of the genes associated with susceptibility to atopic dermatitis. Although it is known to be expressed in murine skin and hair
Mitoma, Chikage, Nakahara, Takeshi, Uchi, Hiroshi, Ito, Takamichi, Inatomi, Yusuke, Ide, Takatoshi, Jinnai, Shunichi, Jinnai, Naomi, Iwasaki, Nahoko, Sakamoto, Keiko, Kimura, Nanae, Maeda, Ayami, Kuma, Yuki, Maehara, Eriko, Tsutsumi, Midori, Nakahara, Makiko, Kido, Makiko, Hirota, Tomomitsu, Tamari, Mayumi, Furue, Masutaka   +19 more
openaire   +2 more sources

[Torre-Muir syndrome. Sebaceous gland neoplasms, keratoacanthomas, multiple internal cancers and heredity].

Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1982
The Torre-Muir syndrome includes multiple sebaceous neoplasms and keratoacanthomas, as well as multiple internal malignancies. We describe three cases of this unusual association which has not previously been reported in the German-speaking literature. The Torre-Muir syndrome appears to have a close connection to the cancer family syndrome [17, 34].
W I, Worret, W H, Burgdorf, A, Fahmy, J, Pitha   +3 more
openaire   +1 more source