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Journal articles on the topic 'Cartilaginous metaplasia'

Author: Grafiati

Published: 28 May 2022

Last updated: 30 July 2025

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1

Lee, A. H. S., and A. D. Ramsay. "Cartilaginous metaplasia of the epiglottis." Journal of Laryngology & Otology 104, no. 11 (1990): 903–4. http://dx.doi.org/10.1017/s0022215100114318.

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AbstractMetaplastic elastic cartilaginous tissue has been described in the vocal cord, vestibular fold and ventricle of the larynx. This report documents a case in which cartilaginous metaplasia developed in the soft tissue of the epiglottis following an episode of epiglottitis.

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2

KARADAĞ, Burak, Gül ALKAN BÜLBÜL, Betül ÇELİK, Tangül BULUT, and Barış MÜLAYİM. "Cartilaginous Metaplasia in Uterine Leiomyoma." Turkiye Klinikleri Journal of Case Reports 27, no. 3 (2019): 122–25. http://dx.doi.org/10.5336/caserep.2018-63727.

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3

Kotru, Mrinalini, Richa Gupta, Seema Aggarwal, Sonal Sharma, and Arati Bhatia. "Cartilaginous metaplasia in uterine leiomyoma." Archives of Gynecology and Obstetrics 280, no. 4 (2009): 671–73. http://dx.doi.org/10.1007/s00404-009-0970-y.

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4

Mujeeb, Madeeha, Jasmeen Tabassum, Naushaba Tazeen, Idrees Afroze, and Imtiyaz Khan. "Cartilaginous metaplasia of thyroid nodule." Journal of Medical and Allied Sciences 15, no. 1 (2025): 92. https://doi.org/10.5455/jmas.214579.

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Adenomatous goiter is the most common form of thyroid disease. Although degenerative changes like fibrosis, calcification, cystic changes and hemorrhagic tissue are commonly found, cartilaginous metaplasia is an unusual phenomenon in the thyroid gland. Heterotopic cartilage formation is a very rare finding in both neoplastic and non-neoplastic lesions. Only 2 cases have been reported so far. Here we present a case of a 65-year-old female who presented with a midline swelling in her neck for 2 months associated with difficulty in swallowing. The lymph nodes were not palpable and there were no p

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5

Hediger, Sebastian, Sylvia Höller, and Konrad Mende. "A Rare Finding in Dupuytren’s Disease - Heterotopic Ossification." Journal of Hand Surgery (Asian-Pacific Volume) 25, no. 04 (2020): 513–14. http://dx.doi.org/10.1142/s2424835520720194.

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We present the case of a severe and long-standing Dupuytren’s contracture where intraoperatively an ossified nodule was encountered within the diseased tissue. Histologically palmar fibromatosis in contact with cartilaginous tissue with central ossification could be confirmed, compatible with metaplasia. Our finding suggests that metaplastic activity inherent to longstanding, severely diseased Dupuytren’s tissue can lead to heterotopic ossification.

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6

Caggiati, A., and M. Franceschini. "Cartilaginous metaplasia of varicose veins: a case report." Phlebology: The Journal of Venous Disease 28, no. 3 (2013): 165–67. http://dx.doi.org/10.1258/phleb.2011.011078.

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Cartilaginous metaplasia of superficial veins was found in a 64-year-old woman who underwent surgery for varicose veins. At operation, some varicose veins of the medial thigh were semi-rigid and fibroelastic to the touch. Histology revealed that half the lumen was occupied by chondroid tissue. The other half was obliterated by fibrous tissue, typical of post-thrombotic involution. Possible causes of cartilaginous metaplasia are briefly discussed.

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7

Moulonguet, Isabelle, Sophie Goettmann, and Ines Zaraa. "Superficial Acral Fibromyxoma With Cartilaginous Metaplasia." American Journal of Dermatopathology 41, no. 4 (2019): 316–17. http://dx.doi.org/10.1097/dad.0000000000001103.

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8

Grunwald, M. H., A. Rothem, and E. J. Feuerman. "Metastatic Malignant Melanoma with Cartilaginous Metaplasia." Dermatology 170, no. 5 (1985): 249–52. http://dx.doi.org/10.1159/000249542.

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9

Khalluf, Edgar, Barry R. DeYoung, and Paul E. Swanson. "Soft Tissue Leiomyoma With Cartilaginous Metaplasia." International Journal of Surgical Pathology 1, no. 4 (1994): 235–38. http://dx.doi.org/10.1177/106689699400100404.

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10

ANDREW, J. G. "Calcification in Dupuytren’s Disease: A Report of Two Cases." Journal of Hand Surgery 12, no. 2 (1987): 277–78. http://dx.doi.org/10.1016/0266-7681_87_90033-7.

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Two cases are presented of calcification within Dupuytren’s tissue. Histological appearances of the tissue showed both cartilaginous and osseous metaplasia. This indicates that fibroblasts in Dupuytren’s Disease may undergo this type of metaplasia in a similar fashion to fibroblasts elsewhere.

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11

Iiyama, Naruhiko, Tatsuhiko Henmi, Yoshiji Kanematsu, Kouichi Sairyo, and Sadao Shinomiya. "Huge Lipoma with Cartilaginous and Osseous Metaplasia." Orthopedics & Traumatology 44, no. 3 (1995): 1150–53. http://dx.doi.org/10.5035/nishiseisai.44.1150.

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12

Groom, Debra A., and William R. Starke. "Cartilaginous Metaplasia in Calcific Aortic Valve Disease." American Journal of Clinical Pathology 93, no. 6 (1990): 809–12. http://dx.doi.org/10.1093/ajcp/93.6.809.

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13

Hilal, H., O. Soussi, H. Arbouni, et al. "Teno-Synovial Chondromatosis: A Radiological Case Report with Review of the Literature." Scholars Journal of Medical Case Reports 10, no. 7 (2022): 684–86. http://dx.doi.org/10.36347/sjmcr.2022.v10i07.020.

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Teno-synovial chondromatosis is an extra-articular cartilaginous or osteo-cartilaginous multinodular proliferation by metaplasia of synovial tissue. It can be primary (Reichel-Jones-Henderson syndrome) or secondary (trauma, arthritis, neuro-arthropathy...). We report the case of an extra-articular teno-synovial osteochondromatosis of the flexors of the 3rd finger by reviewing the different data in the literature.

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14

Nagase, Mamiko, Asuka Araki, Noriyoshi Ishikawa, et al. "Tenosynovial Giant Cell Tumor, Localized Type With Extensive Chondroid Metaplasia: A Case Report With Immunohistochemical and Molecular Genetic Analysis." International Journal of Surgical Pathology 28, no. 4 (2019): 447–53. http://dx.doi.org/10.1177/1066896919889672.

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Tenosynovial giant cell tumor (TSGCT) of localized type is a common disease occurring mostly in the hands. Diagnosis of this tumor is relatively easy to render with hematoxylin-eosin–stained sections as compared with that of TSGCT of diffuse type. However, very rare cases with chondroid metaplasia that have recently been reported mainly in diffuse type can make pathological differentiation from soft tissue cartilaginous tumors extremely difficult. In this article, the authors present the second reported case of TSGCT of localized type showing extensive chondroid metaplasia. Pathological interp

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15

Kitagaki, M., T. Suwa, M. Yanagi, and K. Shiratori. "Auricular chondritis in young ear-tagged Crj:CD(SD)IGS rats." Laboratory Animals 37, no. 3 (2003): 249–53. http://dx.doi.org/10.1258/002367703766453100.

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Gross and histopathological features of auricular chondritis in young Crj:CD(SD)IGS rats were examined. Although the rats were identified with metallic ear tags on the right pinnae, auricular chondritis was also observed on the contralateral (left) ear in some animals. Histopathologically, the lesions were characterized by granulomatous inflammation with destruction of the normal cartilaginous plate, formation of new cartilaginous nodules and osseous metaplasia. Proliferative cell nuclear antigen (PCNA) positive cells were present predominantly in chondrocytes found in the centre of the newly-

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16

Szymanski, Linda J., and Linda M. Ernst. "Cartilaginous Metaplasia Involving the Atrioventricular Node and Bundle of His Contributing to Sudden Early Neonatal Death." Pediatric and Developmental Pathology 23, no. 4 (2019): 312–16. http://dx.doi.org/10.1177/1093526619892352.

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Cartilaginous metaplasia involving the atrioventricular (AV) node is an uncommon entity that may cause sudden cardiac death secondary to dysrhythmias. We report 2 autopsy cases of full-term male newborns: 1 stillborn and 1 live-born, with antemortem bradycardia who died in the peripartum period. An examination of the cardiac conduction system in both cases demonstrated extensive cartilaginous metaplasia of the central fibrous body and involvement of the AV node and bundle of His. The cases highlight the recognition of cardiac conduction system anomalies as a cause of sudden perinatal death. In

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17

HAYASHI, Hironori, Tomohiko HAYASHI, Nagayoshi OTA, and Masayuki ITO. "A CASE OF BREAST CANCER WITH CARTILAGINOUS METAPLASIA." Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) 64, no. 8 (2003): 1864–67. http://dx.doi.org/10.3919/jjsa.64.1864.

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18

TOMITA, Hiroyuki, Hidenori TANAKA, Hiroshi TUYA, and Kiichi MIYA. "A CASE OF BREAST CANCER WITH CARTILAGINOUS METAPLASIA." Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) 65, no. 5 (2004): 1201–4. http://dx.doi.org/10.3919/jjsa.65.1201.

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19

YOSHIMOTO, Naoko, Ritsuko IMAI, Nobuyuki TANAKA, Tatsunari SATAKE, Yoshikazu MIZOGUCHI, and Hideto IWAFUCHI. "A breast cancer with cartilaginous and osseous metaplasia." Journal of the Japanese Society of Clinical Cytology 49, no. 6 (2010): 419–24. http://dx.doi.org/10.5795/jjscc.49.419.

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20

Vyas, Dr KC, Dr Gaurav Wadhawan, Dr Preethi Agarwal, Dr Suraj Jain, and Dr Shashi Sujanani. "Cartilaginous metaplasia in giant fibrolipoma - arare case report." Surgical Update: International Journal of Surgery and Orthopedics 3, no. 4 (2017): 127–29. http://dx.doi.org/10.17511/ijoso.2017.i04.06.

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21

Smith, J. D., A. N. Hamir, and J. J. Greenlee. "Cartilaginous Metaplasia in the Sclera of Suffolk Sheep." Veterinary Pathology 48, no. 4 (2010): 827–29. http://dx.doi.org/10.1177/0300985810382669.

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22

Callahan, Katherine S., Steve C. Eberhardt, Robert E. Fechner, and Lisa A. Cerilli. "Desmoplastic fibroma of bone with extensive cartilaginous metaplasia." Annals of Diagnostic Pathology 10, no. 6 (2006): 343–46. http://dx.doi.org/10.1016/j.anndiagpath.2006.03.016.

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23

Qiao, Jian-Hua, Michael C. Fishbein, Linda L. Demer, and Aldons J. Lusis. "Genetic Determination of Cartilaginous Metaplasia in Mouse Aorta." Arteriosclerosis, Thrombosis, and Vascular Biology 15, no. 12 (1995): 2265–72. http://dx.doi.org/10.1161/01.atv.15.12.2265.

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24

Yoichi, Takuya, Takeshi Nagashima, Hiroshi Yagata, et al. "Breast cancer with cartilaginous and/or osseous metaplasia." Breast Cancer 16, no. 3 (2009): 234–37. http://dx.doi.org/10.1007/s12282-008-0090-8.

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25

Oda, Kinoshita, Tamiya, Iwamoto, and Tsuneyoshi. "Extraskeletal primitive neuroectodermal tumour with massive osteo-cartilaginous metaplasia." Histopathology 36, no. 2 (2000): 188–91. http://dx.doi.org/10.1046/j.1365-2559.2000.0866j.x.

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26

Patil, SunitaB, SeemaS More, and Shilpa Narchal. "Endometrial cartilaginous metaplasia: A case report with literature review." Journal of Mid-life Health 4, no. 3 (2013): 195. http://dx.doi.org/10.4103/0976-7800.118994.

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27

Ayesha, Sajjad, Shah Mehmood Amna, Tasneem Khattak Maria, et al. "Metaplastic Meningioma Presenting with Anemia in A Young Boy Case Report and Review of the Literature." International Journal of Innovative Science and Research Technology 8, no. 3 (2023): 2141–45. https://doi.org/10.5281/zenodo.7811122.

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Meningioma is the most common extra-axial, Dura-based tumor of the central nervous system. These tumors often present in middle to late adult life, especially in women, and account for 15% - 30% of all intracranial tumors(1). Incidence rate of 18.69 and 0.16 per 100,000 is recorded for patients above 40 years and 0-19 years age respectively(2). The World Health Organization (WHO) in its 2021 classification divides meningioma into Grade I (benign), Grade II (atypical), and Grade III (anaplastic) variants. It further subclassifies grade I meningioma into 9 subtypes: meningothelial, fibrous, tran

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28

Davidson, EB, SM Griffey, PB Vasseur, and SL Shields. "Histopathological, radiographic, and arthrographic comparison of the biceps tendon in normal dogs and dogs with biceps tenosynovitis." Journal of the American Animal Hospital Association 36, no. 6 (2000): 522–30. http://dx.doi.org/10.5326/15473317-36-6-522.

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In dogs surgically treated for biceps tenosynovitis, the most common histopathological findings were fibrosis and collagen degeneration (n=13), synovial villous or vascular hyperplasia (n=10), lymphocytic-plasmacytic infiltrates (n=10), cartilaginous metaplasia (n=8), and ischemic necrosis (n=5). Degree of histopathological changes was associated with degree (p equals 0.000), but not duration (p equals 0.543), of lameness. Furthermore, there was no association between histopathological changes and age or radiographic and arthrographic findings. Cartilage metaplasia was the only histopathologic

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29

NARITA, Hiroshi, Futoshi TERANISHI, Nobuko YAMAMORI, et al. "A CASE OF BREAST CANCER WITH OSSIFEROUS AND CARTILAGINOUS METAPLASIA." Journal of the Japanese Practical Surgeon Society 55, no. 9 (1994): 2255–60. http://dx.doi.org/10.3919/ringe1963.55.2255.

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30

Fukuoka, Tatsunari, Yoshinari Ogawa, Mamiko Takii, et al. "Two Cases of Breast Cancer with Cartilaginous and Osseous Metaplasia." Nihon Gekakei Rengo Gakkaishi (Journal of Japanese College of Surgeons) 35, no. 6 (2010): 883–88. http://dx.doi.org/10.4030/jjcs.35.883.

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31

Kato, Aya, Kazuyuki Tani, Hirotaka Nakayama, Ryuji Shiraishi, Yasushi Rino, and Munetaka Masuda. "A Case of Breast Cancer with Cartilaginous and Osseous Metaplasia." Nihon Gekakei Rengo Gakkaishi (Journal of Japanese College of Surgeons) 39, no. 5 (2014): 865–69. http://dx.doi.org/10.4030/jjcs.39.865.

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32

EMOTO, Takashi, Kiyoshi YOSHIKAWA, Masahiro FUJIKAWA, Makoto FUJII, Eisaku HAMADA, and Kiyoshi KAWANO. "A case of breast cancer with cartilaginous and osseous metaplasia." Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) 63, no. 2 (2002): 316–19. http://dx.doi.org/10.3919/jjsa.63.316.

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33

MURAISHI, Yoshie, Tomoko KAWABATA, Masashi FUJITA, et al. "A case of breast carcinoma with cartilaginous and osseous metaplasia." Journal of the Japanese Society of Clinical Cytology 48, no. 1 (2009): 27–31. http://dx.doi.org/10.5795/jjscc.48.27.

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34

MAEDA, Yuriko, Saemi OHSHIRO, Shota SAGA, et al. "A case of breast carcinoma with cartilaginous and osseous metaplasia." Journal of the Japanese Society of Clinical Cytology 53, no. 2 (2014): 132–37. http://dx.doi.org/10.5795/jjscc.53.132.

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35

Ninomiya, Jun, Tetsunari Oyama, Jun Horiguchi, et al. "Two case of breast cancer with cartilaginous and osseous metaplasia." Breast Cancer 12, no. 1 (2005): 52–56. http://dx.doi.org/10.2325/jbcs.12.52.

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36

Kijima, Yuko, Yoshihisa Umekita, Heiji Yoshinaka, et al. "A case of breast carcinoma with cartilaginous and osseous metaplasia." Breast Cancer 13, no. 2 (2006): 214–19. http://dx.doi.org/10.2325/jbcs.13.214.

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37

Altamirano, E., and R. Drut. "Extrahepatic biliary atresia with cartilaginous metaplasia in the gallbladder remnants." Journal of Clinical Pathology 61, no. 8 (2008): 965–66. http://dx.doi.org/10.1136/jcp.2006.045831.

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38

Speer, M. Y. "Smooth muscle cells in pathogenesis of vascular medial cartilaginous metaplasia." Cardiovascular Research 90, no. 1 (2011): 1–2. http://dx.doi.org/10.1093/cvr/cvr047.

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39

MIURA, Daishu, Noriyuki SUZUKI, and Hideki NAKAZAWA. "BREAST CANCER WITH CARTILAGINOUS AND OSSEOUS METAPLASIA-A CASE REPORT-." Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) 61, no. 5 (2000): 1159–63. http://dx.doi.org/10.3919/jjsa.61.1159.

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40

Terazaki, Carlos Renato Ticianelli, Cesar Rodrigo Trippia, Carlos Henrique Trippia, Maria Fernanda Sales Ferreira Caboclo, and Carla Regina Miranda Medaglia. "Synovial chondromatosis of the shoulder: imaging findings." Radiologia Brasileira 47, no. 1 (2014): 38–42. http://dx.doi.org/10.1590/s0100-39842014000100013.

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Synovial chondromatosis is a benign condition characterized by synovial proliferation and metaplasia, with development of cartilaginous or osteocartilaginous nodules within a joint, bursa or tendon sheath. In the shoulder, synovial osteochondromatosis may occur within the glenohumeral joint and its recesses (including the tendon sheath of the biceps long head), and in the subacromial-deltoid bursa. Such condition can be identified either by radiography, ultrasonography or magnetic resonance imaging, showing typical features according to each method. Radiography commonly shows ring-shaped calci

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41

Gigis, Ioannis, and Panagiotis Gigis. "Fibrolipoma with Osseous and Cartilaginous Metaplasia of Hoffa’s Fat Pad: A Case Report." Case Reports in Orthopedics 2012 (2012): 1–5. http://dx.doi.org/10.1155/2012/547963.

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The most common benign tumors of the mesenchyme are the lipomas. Benign fatty tumors can arise in any location in which fat is present. Fibrolipomas are characterised by fat modules. Most patients affected by such tumors are in the fifth or sixth decade of life. When very close to vital structures such as joints, they may cause functional limitations as well as pain. Osseous and chondroid metaplasia can infrequently manifest after chronic persistence. Given the rarity of this condition, a case of a big fibrolipoma of Hoffa’s fat pad with osseous and cartilaginous metaplasia is reported. A 44-y

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42

SHUDO, Yasuhiro, Toyokazu AONO, Yasuhiro TANAKA, and Shouki MIKATA. "A RARE CASE OF BREAST CARCINOMA WITH CARTILAGINOUS AND OSSEOUS METAPLASIA." Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) 66, no. 5 (2005): 1020–22. http://dx.doi.org/10.3919/jjsa.66.1020.

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43

KIMURA, Yoichi, Kazuo INAMOTO, Yuka KANZAKI, et al. "A case of (breast) carcinoma with cartilaginous and/or osseous metaplasia." Journal of the Japanese Society of Clinical Cytology 39, no. 6 (2000): 493–96. http://dx.doi.org/10.5795/jjscc.39.493.

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44

Nakaya, Takeo, Taiju Hyuga, Yukichi Tanaka, et al. "Renal dysplasia characterized by prominent cartilaginous metaplasia lesions in VACTERL association." Medicine 96, no. 15 (2017): e6499. http://dx.doi.org/10.1097/md.0000000000006499.

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45

Yih, Wei-Yung, and John L. Krump. "Odontogenic Keratocyst in the Nasopalatine Duct Associated With Mural Cartilaginous Metaplasia." Journal of Oral and Maxillofacial Surgery 63, no. 9 (2005): 1382–84. http://dx.doi.org/10.1016/j.joms.2005.05.305.

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46

Anderson, W. I., and D. W. Scott. "Cartilaginous metaplasia associated with a basal cell tumour in a dog." Journal of Comparative Pathology 100, no. 1 (1989): 107–9. http://dx.doi.org/10.1016/0021-9975(89)90096-0.

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47

Hong, Ki-Eun, Jun Park, Ji-Eon Yun, et al. "A rare case of temporomandibular joint synovial chondromatosis with cranial base extension." Journal of The Korean Dental Association 59, no. 12 (2021): 734–40. http://dx.doi.org/10.22974/jkda.2021.59.12.004.

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Synovial chondromatosis is an uncommon benign lesion in which the synovial membrane within the joint forms cartilaginous nodules and loose bodies due to cartilaginous metaplasia. It is rare to develop in the temporomandibular joint, and may be accompanied by cranial base expansion or temporal bone morbidity. A 41-year-old male patient visited our hospital complaining of preauricular pain and crepitus. On CT and MRI, increased synovial fluid in the joint cavity, loose body, temporal bone erosion and cranial base expansion were observed. It was diagnosed as synovial chondromatosis through imagin

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48

Jbara, O., D. Laoudiyi, K. Chbani, and S. Salam. "Synovial Chondromatosis of the Ankle in a Child." SAS Journal of Medicine 9, no. 04 (2023): 367–69. http://dx.doi.org/10.36347/sasjm.2023.v09i04.030.

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Synovial chondromatosis is a cartilaginous metaplasia of the residual stroma of the synovial tissue of the joint. Its main characteristic is the formation of cartilaginous nodules in the synovium and in the joint space (loose bodies). It usually appears between the ages of 30 and 50 and is rare in children. It presents as a monoarticular lesion affecting large joints such as the knee, hip and elbow, and rarely the ankle. The main symptoms are pain, swelling and limited mobility in the affected joints. Diagnosis is based on X-rays, CT scans and magnetic resonance imaging. In this case report, w

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49

Lahrach, Mohamed, Khaoula Nini, Mohamed Koussay Hattab, Zakaria Aziz, Mohamed Elbouihi, and Nadia Mansouri Hattab. "Synovial Chondromatosis of the Temporomandibular Joint with Extension to the Glenoid Fossa." SAS Journal of Surgery 9, no. 04 (2023): 269–74. http://dx.doi.org/10.36347/sasjs.2023.v09i04.012.

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Synovial chondromatosis is a rare pathology that affects the large joints, it is exceptional in TMJ, it is related to a synovial metaplasia with production of cartilaginous bodies in the temporomandibular joint (TMJ) , its slow evolution and its non-specific clinical presentation are the causes of the diagnostic delay that characterizes this pathology; We present a case of synovial chondromatosis of the TMJ in a 38 year old patient, in whom the CT scan showed a cartilaginous tumor of the TMJ with erosion of the glenoid fossa without intracranial extension, The biopsy with anatomopathological s

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50

Senapati, Swagatika, Shruti Mahawar, and Krushna Chandra Pani. "Osseocartilaginous metaplasia in the Endometrium: A Rare Reversible Cause of Secondary Infertility." Annals of Pathology and Laboratory Medicine 9, no. 4 (2022): C38–40. http://dx.doi.org/10.21276/apalm.3151.

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Osteo-cartilaginous metaplasia in endometrium is an infrequent finding and usually presents with secondary infertility. This is a benign entity and usually associated with a previous history of abortion. It can be treated successfully with hysteroscopy and henceforth reverting infertility. Awareness of this entity is important in order to avoid overdiagnosis of mixed Mullerian tumor of the endometrium followed by hysterectomy. Herein, we present one such case of a 28-year-old female who presented with secondary infertility.

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