Results 211 to 220 of about 2,852,439 (245)

Tumoral Calcinosis in the Neck

Otolaryngology–Head and Neck Surgery, 1987
Tumoral calcinosis manifests soft-tissue calcification, usually near major joints. It variably includes hyperphosphatemia, elevated 1,25-dihydroxycalciferol, and an affected sibling. Serum calcium, alkaline phosphatase, and parathyroid hormone are normal. Tumoral calcinosis of the head and neck is very rare, but this diagnosis should be considered when
Paul A. Levine, Karen H. Calhoun, William D. Clark, Charles M. Sternberg, Francis B. Quinn, Jason H. Calhoun   +5 more
openaire   +3 more sources

Hyperphosphatemic Familial Tumoral Calcinosis

Southern medical journal (Birmingham, Ala. Print)
Hyperphosphatemic familial tumoral calcinosis is an autosomal recessive condition that requires a multidisciplinary approach, not only to reach an accurate diagnosis but also for treatment.
Margaret Kaszycki, Beija K Villalpando, LaTonya J Hickson, Sarika Rao, Klaas Wierenga, Hillary W Garner, O. Sokumbi, Leila Tolaymat   +7 more
semanticscholar   +1 more source

Hyperphosphatemic familial tumoral calcinosis in a dancer

PM & R : the journal of injury, function, and rehabilitation, 2022
A healthy 51-year-old female dancer and choreographer presented to a sports medicine clinic with 2 years of bilateral lower extremity pain. The pain was described by the patient as being located between the knees and ankles and was aggravated with ...
Wei-Xian Li, Jeremy Stanek
semanticscholar   +1 more source

Hyperphosphatemia and Tumoral Calcinosis

Annals of Internal Medicine, 1968
Abstract Two teenage negro brothers with chronic hyperphosphatemia, one of whom exhibited heterotopic calcifications around large joints, underwent studies of phosphate metabolism.
John F. Wilber, Eduardo Slatopolsky
openaire   +3 more sources

Tumoral Calcinosis in Scleroderma

The Journal of Dermatology, 1989
AbstractA 36‐year‐old female patient with scleroderma/Sjögren's syndrome developed multiple cystic tumors on the dorsal aspect of her left hand, right elbow, and left shoulder joint two years after the onset of scleroderma. Histologically, amorphous eosinophilic substances located in subcutaneous tissue showed a strong positive reaction to PTAH and ...
Kiyoshi Nishioka, Ichiro Katayama, Kazunori Higashi, Hideki Mukai, Shigeo Nishiyama   +4 more
openaire   +3 more sources

Tumoral calcinosis of the nose

The Journal of Laryngology & Otology, 1984
A rare and interesting case of tumoral calcinosis of the nose causing external nasal deformity and managed by surgical excision and corrective rhinoplasty is presented.
K. J. S. Ahluwalia, P. C. Chamyal
openaire   +3 more sources

Tumoral Calcinosis with an Atypical Presentation in the Foot: A Case Report.

Journal of the American Podiatric Medical Association (Print)
Tumoral calcinosis is a rare disorder defined as the development of periarticular calcified masses, typically surrounding large joints, although they may occur in the foot.
Thomas Ehlers, Kenny Luong, Kristina Karlic, Matrona Giakoumis   +3 more
semanticscholar   +1 more source

Familial hyperphosphatemic tumoral calcinosis in an unusual and usual sites and dramatic improvement with the treatment of acetazolamide, sevelamer and topical sodium thiosulfate

Journal of Pediatric Endocrinology & Metabolism (JPEM), 2021
Objectives Familial hyperphosphatemic tumoral calcinosis is a rare disorder characterized by hyperphosphatemia with recurrent ectopic periarticular calcifications, in addition to other visceral and vascular manifestations, without any inflammatory or ...
Merve Emecen Şanlı, A. Kılıç, Ekin Aktaşoğlu, A. Inci, I. Okur, F. Ezgu, L. Tumer   +6 more
semanticscholar   +1 more source

Tumoral calcinosis in an infant

Skeletal Radiology, 1996
We report tumoral calcinosis, an uncommon disease of uncertain origin, in an infant-only the sixth instance of the disease reported in this age group. The radiologic features are typical as illustrated by three modalities. The clinical, radiologic and pathologic features are discussed along with comments concerning possible etiologies and management.
Prasit Nimityongskul, B. G. Brogdon, Patti H. Richardson, Yih-Ming Yang   +3 more
openaire   +3 more sources

Tumoral calcinosis due to severe hyperphosphatemia and secondary hyperparathyroidism without vascular calcification in a hemodialysis patient.

Clinical Nephrology, 2021
We report a case of a 32-year-old man who was undergoing chronic hemodialysis and had hyperphosphatemia and secondary hyperparathyroidism (SHPT) with multiple tumoral calcinosis (TC) lesions refractory to drug therapy.
Tomohiro Saito, Masahide Mizobuchi, Toma Hamada, Motonori Sugiyama, Nozomi Miyazawa, Tomoki Morikawa, Kei Matsumoto, O. Yoshitake, Takeshi Aoki, M. Murakami, H. Honda   +10 more
semanticscholar   +1 more source