Results 11 to 20 of about 111 (52)

Pseudoxanthomatous mastocytosis [PDF]

open access: yesInternational Journal of Dermatology, 2007
A 50‐year‐old woman presented with itchy, multiple, flat, yellowish, waxy papules and plaques diffusely involving her face, trunk, and upper extremities for 5 years (Fig. 1). Itching was moderate to severe in intensity and was episodic, without any identifiable aggravating or relieving factors.
Neeraj, Srivastava   +2 more
openaire   +3 more sources

Adult onset of xanthelasmoid mastocytosis: Report of a rare entity

open access: yesIndian Journal of Dermatology, 2016
Xanthelasmoid or pseudoxanthomatous mastocytosis is an extremely rare variant of diffuse cutaneous mastocytosis. Herein, we describe an adult male with cutaneous mastocytosis showing multiple widespread yellowish ovoid papules like eruptive xanthoma.
Nafiseh Sadat Nabavi   +4 more
doaj   +2 more sources

When the Tube Speaks First: Pseudoxanthomatous Salpingitis Providing a Clue to Underlying Endometriosis

open access: yesJournal of Medical Sciences and Health
Pseudoxanthomatous salpingitis (PXS) is a rare, non-specific inflammatory condition of the fallopian tube, characterized by the presence of hemosiderin-laden macrophages within dilated tubal plicae. We report the case of a 40-year-old woman presenting with lower abdominal pain with imaging features suggestive of bilateral hemorrhagic ovarian cysts and ...
Archana Shetty
exaly   +2 more sources

Pseudoxanthomatous Salpingitis Masquerading as a Tubo-Ovarian Malignancy in a Patient With Endometriosis: A Rare Case Report

open access: yesInternational Journal of Reproduction, Contraception, Obstetrics and Gynecology
Pseudoxanthomatous salpingitis (PXS), also known as pigmentosis tubae, is an extremely rare benign inflammatory condition of the fallopian tube characterised by the presence of lipofuscin- and hemosiderin-laden macrophages within the lamina propria. Owing to its gross appearance and radiological findings, it may closely mimic tubo-ovarian malignancy ...
Nancy Thind   +4 more
exaly   +2 more sources

Xanthogranulomatous endometritis: A case report and literature review

open access: yesClinical Case Reports, Volume 9, Issue 6, June 2021., 2021
Xanthogranulomatous endometritis is a rare benign pathology mimicking endometrial carcinoma. Abstract Xanthogranulomatous endometritis is a rare benign pathology mimicking endometrial carcinoma.
Philippe Merviel   +9 more
wiley   +1 more source

Clinical features in individuals with GACI and/or hypophosphatemic rickets, or PXE.

open access: yes, 2022
Patient #1: (a1) Prenatal ultrasound of the upper abdomen at 35 weeks of gestation showed calcification along the wall of the aorta (green arrows) and proximal superior mesenteric artery (green arrowheads); (a2) Chest X-ray (inverted) at three days after
Amir Hossein Saeidian (12525125)   +11 more
core   +2 more sources

Coexistence of two types of clinical lesions in childhood-onset mastocytosis

open access: yes, 2011
The vast majority of mastocytosis appear in childhood, urticaria pigmentosa (UP) and mastocytomas being the most common types. Terms such as "xanthelasmoid mastocytosis", "pseudoxanthomatous mastocytosis" or "nodular mastocytosis" have been introduced in
Pérez-Pérez, Lidia   +5 more
core   +4 more sources

Xanthogranulomatous Salpingooophoritis: The Youngest Documented Case Report

open access: yesCase Reports in Obstetrics and Gynecology, Volume 2015, Issue 1, 2015., 2015
Background. Xanthogranulomatous inflammation is an uncommon affection of the female genital tract. The youngest case reported of xanthogranulomatous salpingooophoritis in literature was by Shilpa et al. in 2013 in an eighteen‐year‐old female. Case Report.
Harshawardhan Tanwar   +5 more
wiley   +1 more source

Sex Differences Associated with Primary Biliary Cirrhosis

open access: yesJournal of Immunology Research, Volume 2012, Issue 1, 2012., 2012
Primary biliary cirrhosis (PBC) is a cholestatic liver disease of autoimmune origin, characterised by the destruction of small intrahepatic bile ducts. The disease has an unpredictable clinical course but may progress to fibrosis and cirrhosis. The diagnostic hallmark of PBC is the presence of disease‐specific antimitochondrial antibodies (AMA), which ...
Daniel S. Smyk   +8 more
wiley   +1 more source

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