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Journal articles on the topic 'Osseous metaplasia'

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1

Lee, Eun-Joo, and Kyu-Shik Jeong. "A Rare Case of Osseous Metaplasia in Canine Leiomyoma and Plasticity of Smooth Muscle Cell." Acta Veterinaria 72, no. 2 (2022): 268–75. http://dx.doi.org/10.2478/acve-2022-0021.

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Abstract Metaplasia is a transformation of one mature cell type to other kinds of mature cells. Metaplasia is hardly detected in benign tumors, whereas it is frequently observed in malignant tumors. In this study, we report the first case of osseous metaplasia in canine leiomyoma. The region of osseous metaplasia was highly eosinophilic and had various sizes of distinct lacunae. The osseoid material was confirmed by Von Kossa staining. Except for the osseous metaplasia, the mass presented typical features of leiomyoma without any histopathological features of malignancy. The characteristics of
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2

Rajashree Pradhan, Madhumita Paul, Arindam Bandopadhyay, and Sajeeb Mondal. "Osseous Metaplasia of the Breast: A Series of Rare Cases." Indian Journal of Public Health Research & Development 15, no. 2 (2024): 287–89. http://dx.doi.org/10.37506/qmcvn730.

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Osseous metaplasia is a reversible condition in which non-osseous soft tissue is replaced by bone. This is most commonly seen in musculoskeletal system and central nervous system. Osseous metaplasia in breast is a rare event. In this case series, we have reported 4 cases of osseous metaplasia of breast. 1 case of Osseous metaplasia in benign phyllodes tumor, 1 case of Osseous metaplasia in fibroadenoma, 1 case of Osseous metaplasia in invasive breast carcinoma and 1 extremely rare case of Osseous metaplasia of breast presenting as breast lump without any other associated pathology. Since osseo
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3

Alrowaiei, Fatima, and Mohammed Awadh. "Juvenile Polyp with Osseous Metaplasia Presenting with Fecal Incontinence in Young Patient : Case Report of Unusual Presentation." JOURNAL OF THE BAHRAIN MEDICAL SOCIETY 37, no. 1 (2025): 13–16. https://doi.org/10.26715/jbms.37_1_2.

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Osseous metaplasia is rare in colorectal lesions and exceedingly rare in colonic polyps. We present a case report of rectal juvenile polyp with stromal osseous metaplasia in a 21-year-old male who presented with fecal incontinence episodes throughout the day and night over the past 2 years. The patient underwent a colonoscopy and polypectomy, which showed a juvenile polyp with osseous metaplasia. The patient’s primary concern was to fully recover postoperatively. Juvenile polyp with osseous metaplasia may be added to the differential diagnosis of patients with fecal incontinence. This work aim
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4

Alam, Md Shahid, and Rajeev Priyadarshi. "Intraocular osseous metaplasia." Indian Journal of Ophthalmology 68, no. 6 (2020): 1175. http://dx.doi.org/10.4103/ijo.ijo_1829_19.

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5

Buch, ArchanaC, YugamV Chopra, PradeepS Jadhav, and PradhanM Pagaro. "Intraocular osseous metaplasia." Medical Journal of Dr. D.Y. Patil University 5, no. 1 (2012): 73. http://dx.doi.org/10.4103/0975-2870.97522.

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6

Landim, Fábio Machado, José Marconi Tavares, Deborah Nunes de Melo Braga, Jose Erialdo da Silva, Joao Bosco Breckenfeld Bastos Filho, and Roney Gonçalves Fechine Feitosa. "Vaginal osseous metaplasia." Archives of Gynecology and Obstetrics 279, no. 3 (2008): 381–84. http://dx.doi.org/10.1007/s00404-008-0706-4.

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7

Singh, Anil Kumar, Priyanka Gogoi, Preeti Diwaker, Bhuvan Adhlakha, and Aishwary Gayatree. "Osseous metaplasia of ovarian cyst: a rare case report." International Surgery Journal 5, no. 9 (2018): 3164. http://dx.doi.org/10.18203/2349-2902.isj20183741.

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Osseous metaplasia has been described at many sites, however previous reports of osseous metaplasia in ovarian lesions are rare. This is most commonly associated with dermoid cyst, osseous metaplasia in stroma rich in serous or mucinous neoplasm and ossification of endometriotic cyst (chocolate cyst). Here The authors report a case of incidental finding of osseous metaplasia in the endometriotic cyst (chocolate cyst) of resected ovary in 42-year-old female who had gone for total abdominal hysterectomy with bilateral salpingo-oophorectomy for provisional diagnosis of AUB.
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8

Bhavya, Gajjela, Sajitha K, and Michelle Mathias. "Benign phyllodes tumor with osseous metaplasia: A rare case report." IP Archives of Cytology and Histopathology Research 8, no. 2 (2023): 134–37. http://dx.doi.org/10.18231/j.achr.2023.031.

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Phyllodes tumors are rare fibroepithelial neoplasms of the breast, classified as benign, borderline, or malignant based on histological features. Osseous metaplasia, characterized by the presence of bone formation within the tumor, is an uncommon finding. This case report highlights the rarity of osseous metaplasia in a benign phyllodes tumor.A 23-year-old female presented with a gradually enlarging lump in the left breast. Mammography and cytological diagnosis were suggestive of giant fibroadenoma. Surgical excision was done and a histopathological diagnosis of benign phyllodes tumor with oss
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9

Priyadarshi, Shivam, and Varshakothari . "Adrenal Myelolipoma with Osseous Metaplasia and Hypercortisolism." New Indian Journal of Surgery 8, no. 1 (2017): 97–99. http://dx.doi.org/10.21088/nijs.0976.4747.8117.19.

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10

Gautam, Himleena, Alaka Goswami, Papari Goswami, and Kamal Kumar Kathar. "Endometrial osseous metaplasia in a case of abnormal uterine bleeding." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 8, no. 11 (2019): 4596. http://dx.doi.org/10.18203/2320-1770.ijrcog20194903.

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Endometrial osseous metaplasia is an uncommon pathology with varied clinical symptoms. Its pathogenesis is not exactly known and has a benign course. Here we present a case of a 42-year-old female with abnormal uterine bleeding who did not respond to medical management. On ultrasonography, suspected endometrial calcification was seen. Patient opted for hysterectomy and the biopsy report showed endometrial osseous metaplasia. Thus, in this case of menometrorrhagia and dysmenorrhoea, the cause was found to be osseous metaplasia.
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11

Funai, Kazuhito, Tomoyuki Yokose, Junji Yoshida, et al. "Thymoma with Osseous Metaplasia." Journal of Computer Assisted Tomography 25, no. 6 (2001): 897–99. http://dx.doi.org/10.1097/00004728-200111000-00012.

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12

International, Journal of Medical Science and Innovative Research (IJMSIR). "Sinonasal polyp with osseous metaplasia – A rare case with review of literature." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 3 (2024): 16–18. https://doi.org/10.5281/zenodo.15401834.

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<strong>Abstract</strong> Inflammatory nasal polypsare quite rare arising from the nasal septum especially with osseous metaplasia. They can extent to the oropharynx, when they are larger in size. We report a case of inflammatory nasal polyp arising from the nasal septum showing osseous metaplasia in a 65year old male patient. Thepolyp was larger in size extending into oropharynx, which resulted in difficulty in swallowing along with nasal obstruction. Surgical excision was done and histopathological examination proved it to be inflammatory nasal polyp with osseous metaplasia.
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13

Nasrallah, Oussama G., Baraa AlJardali, Jose M. El Asmar, Abdallah El Kasti, and Albert El Hajj. "TFE3-rearranged RCC with osseous metaplasia found on bone mass densitometry." Annals of Medicine & Surgery 86, no. 10 (2024): 6198–202. http://dx.doi.org/10.1097/ms9.0000000000002479.

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Introduction and importance: Renal cell carcinoma (RCC) is the most common primary renal malignancy in patients between the ages of 50 and 70. A rare described variant of RCC is transcription factor for immunoglobulin heavy-chain enhancer 3 (TFE3) rearranged RCC. Osseous metaplasia, which refers to the occurrence of normal bone tissue in soft tissue, has been observed in all subtypes of renal cell carcinoma (RCC); however, only three previous case reports have documented the occurrence of osseous metaplasia in TFE3-rearranged RCC. Case presentation: We present a case of a 65-year-old woman pre
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14

Permi, Harish S. "RENAL CELL CARCINOMA WITH OSSEOUS METAPLASIA OCCURRING IN A CONTRACTED KIDNEY - A RARE CASE REPORT." Journal of Health and Allied Sciences NU 03, no. 04 (2013): 137–38. http://dx.doi.org/10.1055/s-0040-1703721.

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AbstractOsseous metaplasia is a rare histologic feature associated with renal cell carcinoma, occurring in a contracted kidney is still rarer. Metaplastic bone formation within the renal tumor gives an appearance similar to that of calcification. It is difficult to distinguish between bone formation and calcification on the basis of radiological imaging alone. Prognostic significance of metaplastic bone formation in renal cell carcinoma is not clear, however some report suggest good prognosis as a result of limitation of tumor spread by bone formation. This case report highlights the occurrenc
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15

Alkhaibary, Ali, Fahd AlSufiani, Ali H. Alassiri, Makki Almuntashri, and Salma Tarik Al Qutub. "Chondro-Osseous Metaplasia in Ependymoma: A Rare Histopathological Finding." Case Reports in Pathology 2020 (May 5, 2020): 1–6. http://dx.doi.org/10.1155/2020/1528698.

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Ependymoma is a circumscribed glioma composed of uniform glial cells with bland nuclei in a fibrillary matrix. It is characterized by the presence of perivascular pseudorosettes. Unusual histopathological findings have rarely been reported in ependymomas, 0.5% of all diagnosed cases. Such unusual and exceedingly rare histological findings include osseous or chondroid metaplasia. To the best of our knowledge, only 15 cases of osseocartilaginous ependymomas have been reported in English literature. We report a 3-year-old boy who presented with ataxia, vomiting, and headache for three months. Rad
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16

Campos, Marta, Marta Xavier, and Maria Elisa Paredes. "Osseous metaplasia of the endometrium - An unusual clinical case." Acta Obstétrica e Ginecológica Portuguesa 18, no. 4 (2024): 316–17. https://doi.org/10.69729/aogp.v18i4a08.

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Endometrial osseous metaplasia is a rare non-neoplastic transformation in which the endometrial stroma is replaced by bone and cartilage. It is more frequently observed after repeated miscarriages and is associated with secondary infertility. The authors report a case of an endometrial osseous metaplasia with an uncommon presentation.
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17

Rodiño Tilve, Verónica, Thomas Maddox, Lorenzo Ressel, and Rob Pettitt. "Osseous Metaplasia of the Transverse Humeral Ligament in a 10-Year-Old Bengal Cat." VCOT Open 05, no. 01 (2022): e6-e10. http://dx.doi.org/10.1055/s-0042-1742472.

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AbstractThis report is of an osseous metaplasia of the transverse humeral ligament and secondary bicipital tenosynovitis in a 10-year-old Bengal cat. Computed tomography revealed the presence of an osseous bridge enclosing the bicipital groove, with ultrasonography confirming partial tear and inflammation of the bicipital tendon. Initial conservative management with intra-articular long-acting steroids failed to provide long-term improvement of clinical signs. Surgical excision of the osseous lesion resulted in complete resolution of lameness after surgery, confirmed by a 1-year follow-up. His
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18

Bychkova, E. Yu, Olga G. Grigoruk, D. O. Kuratov, E. A. Afanasieva, L. M. Bazulina, and N. A. Bykova. "Uncommon case of the acral melanoma with chondro-osseous metaplasia." Russian Journal of Oncology 25, no. 6 (2020): 208–12. http://dx.doi.org/10.17816/1028-9984-2020-25-6-208-212.

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Aim. This study aimed to improve the diagnostics of acral melanoma and investigate tumor morphological features of the chondroid and osseous matrix.&#x0D; Materials and methods. The article presents a clinical case of metastatic acral melanoma with chondroid and osseous metaplasia in a 60-year-old patient. Cytological, histologic, immunohistochemical, and molecular genetic studies were performed.&#x0D; Results. A conglomerate of lymph nodes was noted in the inguinal region of the patient. Oxyphilic chondroid masses and tumor cells with morphological features of sarcoma were revealed using thin
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19

Bychkova, E. Yu, Olga G. Grigoruk, D. O. Kuratov, E. A. Afanasieva, L. M. Bazulina, and N. A. Bykova. "Uncommon case of the acral melanoma with chondro-osseous metaplasia." Russian Journal of Oncology 25, no. 6 (2020): 208–12. http://dx.doi.org/10.17816/1028-9984-2020-25-6-208-212.

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Aim. This study aimed to improve the diagnostics of acral melanoma and investigate tumor morphological features of the chondroid and osseous matrix.&#x0D; Materials and methods. The article presents a clinical case of metastatic acral melanoma with chondroid and osseous metaplasia in a 60-year-old patient. Cytological, histologic, immunohistochemical, and molecular genetic studies were performed.&#x0D; Results. A conglomerate of lymph nodes was noted in the inguinal region of the patient. Oxyphilic chondroid masses and tumor cells with morphological features of sarcoma were revealed using thin
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20

Liu, Xibo, Jinghong Xu, and Lirong Chen. "Colorectal carcinoma with osseous metaplasia." Oncotarget 8, no. 39 (2017): 65407–13. http://dx.doi.org/10.18632/oncotarget.18577.

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21

Handra-Luca, Adriana, Damien Bisseret, Philippe Gorphe, and Nebojsa Arsenovic. "Nasal angioma with osseous metaplasia." Avicenna Journal of Medicine 5, no. 4 (2015): 128. http://dx.doi.org/10.4103/2231-0770.165124.

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22

Van der Merwe, J. P., Igno Siebert, Theunis Frans Kruger, and Dawie Slabbert. "Osseous metaplasia of the endometrium." South African Journal of Obstetrics and Gynaecology 20, no. 1 (2014): 37. http://dx.doi.org/10.7196/sajog.727.

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23

Ortiz-Hidalgo, Carlos, and Javier Baquera-Heredia. "Osseous Metaplasia in Polypoid Cholesterosis." American Journal of Surgical Pathology 24, no. 6 (2000): 895. http://dx.doi.org/10.1097/00000478-200006000-00018.

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24

Papadopoulos, Mario C., Jane Weston, and Adrian B. S. Ball. "Osseous metaplasia in caecal adenocarcinoma." Journal of the Royal Society of Medicine 91, no. 8 (1998): 434–35. http://dx.doi.org/10.1177/014107689809100813.

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25

Liu, Abby Y., Harvey P. Cole, Melissa L. Meldrum-Aaberg, and Hans E. Grossniklaus. "Osseous Metaplasia of the Eyelid." Ophthalmic Plastic and Reconstructive Surgery 30, no. 1 (2014): e9-e10. http://dx.doi.org/10.1097/iop.0b013e3182873d4c.

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26

Sabatini, Luca, Andrew J. Rainey, Walter Tenuwara, and John B. Webb. "Osseous metaplasia of cervical epithelium." BJOG: An International Journal of Obstetrics and Gynaecology 108, no. 3 (2001): 333–34. http://dx.doi.org/10.1111/j.1471-0528.2001.00062.x.

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27

Sabatini, Luca, Andrew J. Rainey, Walter Tenuwara, and John B. Webb. "Osseous metaplasia of cervical epithelium." British Journal of Obstetrics and Gynaecology 108, no. 3 (2001): 333–34. http://dx.doi.org/10.1016/s0306-5456(00)00062-0.

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28

Yoon, Young Doo, Thomas M. Aaberg, Ted H. Wojno, and Hans E. Grossniklaus. "Osseous metaplasia in proliferative vitreoretinopathy." American Journal of Ophthalmology 125, no. 4 (1998): 558–59. http://dx.doi.org/10.1016/s0002-9394(99)80201-3.

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Zisman, Gilat, Rachel F. Brem, and David E. Kardon. "Osseous Metaplasia in the Breast." Journal of Women's Imaging 5, no. 3 (2003): 134–37. http://dx.doi.org/10.1097/00130747-200308000-00008.

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30

Gulec, U. K., H. A. Parlakgumus, E. B. Kilicdag, F. Bolat, and T. Bagis. "Osseous metaplasia of the endometrium." Case Reports 2010, aug17 1 (2010): bcr0420102931. http://dx.doi.org/10.1136/bcr.04.2010.2931.

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31

Stevanovic, Dejan, Vuk Aleksic, Dragos Stojanovic, Nebojsa Mitrovic, Damir Jasarovic, and Zorana Bokun-Vukasinovic. "Osseous metaplasia in an inflammatory polyp of the anal canal: A case report and a review of literature." Srpski arhiv za celokupno lekarstvo 147, no. 3-4 (2019): 211–14. http://dx.doi.org/10.2298/sarh180312037s.

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Introduction. Osseous metaplasia is a heterotopic formation of bone and its appearance in benign gastrointestinal polyps is exceedingly rare. The mechanism responsible for this type of metaplasia is not fully understood, however it seems to be an innocent rare phenomenon. Case outline. We present a case of a 31-year-old male with mesenchimal osseal metaplasia in a large inflamatory polyp measuring 57 ? 23 ? 20 mm in diameter, located in the anal canal region. Conclusion. According to our knowledge, this is the largest gastrointestinal polyp with osseous metaplasia described so far. Although a
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Islam, KM Tarikul, Soumen Samadder, Nazmin Ahmed, Shamsul Alam, Moududul Haque, and ATM Mosharef Hossain. "Psammomatous Thoracic spinal meningioma with osseous metaplasia: A very rare case report." Bangladesh Journal of Neurosurgery 9, no. 2 (2020): 142–45. http://dx.doi.org/10.3329/bjns.v9i2.44890.

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Thoracic spinal psammomatous meningioma is a rare subtype of meningioma. Amongdiverse types of mesenchymal differentiation, osseous metaplasia is found to be stillrarer. We are presenting a new case of thoracic psammomatous spinal meningiomawith osseous metaplasia in a middle aged female which that gives a sense of cancellousbone in the spinal canal. To conclude, meningiomas with osseous metaplasia are veryrare tumors that complicate the surgical removal in certain cases. Ossification, ifpredicted prior to operation with computed tomography reconstruction, makes planningof removal easier. In o
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33

Garcia, Jamile M., Luiz A. S. Silva, Nathalia S. R. Elias, et al. "Bilateral sialocele associated with osseous metaplasia in a dog." Brazilian Journal of Veterinary Pathology 16, no. 3 (2023): 225–27. http://dx.doi.org/10.24070/bjvp.1983-0246.v16i3p225-227.

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Sialocele is a lesion characterized by a cavity filled with saliva and delimited by granulation tissue and is the most commonly observed condition in dogs' salivary glands. A cervical swelling was observed in a male, mixed breed, 12-year-old dog. When punctured, the local was filled with saliva. The animal was referred for sialoadenectomy, and bilateral involvement was observed, with stony material delimiting the sialoceles on both sides. Samples were sent for histopathological examination, which showed cavity areas without epithelial delimitation, with osseous metaplasia and chronic inflammat
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Sampath, Ananyan, Hemalata Panwar, Neelkamal N. A. Kapoor, and Pramod Kumar Sharma. "Osseous metaplasia in a rectal polyp." BMJ Case Reports 16, no. 9 (2023): e254819. http://dx.doi.org/10.1136/bcr-2023-254819.

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Rectal polyps are finger-like projections of the mucosal surface that generally present with complaints of bleeding or mass per rectum. Polyps are classified histopathologically as neoplastic and non-neoplastic. Here, we present one such rare case of a middle-childhood boy who presented with complaints of bleeding per-rectum and revealed a 1.5 cm long rectal polyp. Histopathological examination revealed an osseous change in the rectal polyp. A detailed literature review of reported cases of benign rectal polyps with osseous metaplasia was conducted and consolidated all postulated theories of p
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Zhang, Y., and Y. Nakanishi. "A case of osseous metaplasia in a gastric hyperplastic polyp: An unexpected finding in a common polyp." American Journal of Clinical Pathology 156, Supplement_1 (2021): S69—S70. http://dx.doi.org/10.1093/ajcp/aqab191.145.

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Abstract Introduction/Objective Foveolar hyperplastic polyp is a common gastric polyp characterized by foveolar hyperplasia with erosion, acute and chronic inflammation, granulation tissue formation, and smooth muscle strands extending from the muscularis mucosae. Although foveolar hyperplastic polyps may rarely contain foci of dysplasia or invasive carcinoma, osseous metaplasia/heterotopic bone formation in foveolar hyperplastic polyps of the stomach is extremely rare with a few case reports. Methods/Case Report A 63-year-old female with a history of hypertension, sick sinus syndrome, and Has
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Jagtap, Sunil Vitthalrao. "Ovarian Low-Grade Papillary Serous Cystadenocarcinoma with Osseous Metaplasia- Case Report and Review of Literature." Clinical Pathology & Research Journal 8, no. 1 (2024): 1–5. http://dx.doi.org/10.23880/cprj-16000179.

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Introduction: The stromal osseous metaplasia is extremely rare finding in serous cystadenocarcinoma of the ovary. Case report: A 45-year old female presented with pain in lower abdomen of about 2 months, breathlessness of 10days. On physical examination per abdomen, a large pelvic mass identified. She had pleural and pericardial effusion. Pericardiocentesis was done. Abdomen and pelvis ultrasound revealed a large heterogeneous right adnexal ovarian mass measuring 13.5 × 13.1 × 10.8cm, volume about 916 ml. It was well defined, oval, cystic, partially solid mass, the impression of ovarian neopla
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Mishra, Mona, Neetu Singh, and Rupita Kulshreshtha. "Osseous metaplasia of the endometrium presenting as haematometra: a rare presentation." BMJ Case Reports 17, no. 12 (2024): e262503. https://doi.org/10.1136/bcr-2024-262503.

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Osseous metaplasia of the endometrium is a rare condition involving the bone tissue in the endometrial cavity. Its presence along with haematometra is an infrequent condition and is not reported until now. We present a case of a woman in her mid-30s with primary infertility and secondary amenorrhoea. On evaluation, she was diagnosed with osseous metaplasia, intrauterine synechiae and haematometra. Hysteroscopic removal of bone fragments was done along with synechiolysis which led to the return of menses.
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Makhoba, Aubrey M., and Lorraine du Toit-Prinsloo. "Osseus metaplasia in chronic renal allograft rejection." African Journal of Nephrology 20, no. 1 (2017): 45–47. http://dx.doi.org/10.21804/20-1-900.

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The formation of heterotopic bone tissue outside the skeleton, known as osseous metaplasia, is a well-known phenomenon, but only a handful of cases describe this in renal allografts. We report the case of a 26-year-old female who was admitted to hospital for repair of an arteriovenous fistula of the right arm. Following her demise, the incidental finding of osseous metaplasia in the allograft kidney was made at autopsy. The pathophysiology, histology and possible clinical significance of the lesion are described.
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Bianchi, Simonetta, Giorgio Malatantis, Gaetano Cardona, and Giancarlo Zampi. "Osteogenic Sarcoma of the Breast. A Case Report." Tumori Journal 78, no. 1 (1992): 43–46. http://dx.doi.org/10.1177/030089169207800110.

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A case of primary osteogenic sarcoma of the breast is reported. It should be distinguished from carcinoma with extensive osseous metaplasia. The results of light and electron microscopy including an immunohistochemical study are presented. Immunohistochemical and ultrastructural studies proved that the lesion, in the absence of epithelial differentiation, was a primary osteogenic sarcoma of the breast rather than a carcinoma with extensive osseous metaplasia. Diagnosis may be delayed because the tumor is confused clinically and mammographically with a calcific fibroadenoma.
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Sharma, Rashim, Sudeep Khera, Taruna Yadav, and Mayank Badkur. "Pleomorphic adenoma: Indeed, a versatile tumor." Journal of Cancer Research and Therapeutics 20, no. 5 (2023): 1611–14. http://dx.doi.org/10.4103/jcrt.jcrt_2259_22.

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ABSTRACT Pleomorphic adenoma is the most common and well-studied salivary gland neoplasm. It is a benign tumor most commonly occurring in the parotid gland although it can be seen in other major and minor salivary glands. There is a variety of metaplasia seen in Pleomorphic adenoma most commonly squamous metaplasia, others noted are osseous metaplasia, oncocytic metaplasia, sebaceous metaplasia, and adipocytic metaplasia. Also, at times tyrosine crystalloids are seen. This study discusses a few of the metaplasia and the presence of tyrosine crystals in pleomorphic adenoma. Indeed, this tumor p
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Bavikar, Rupali, and Srishti Malla. "Pulmonary Osseous Metaplasia in an Explant Lung with Interstitial Lung Disease: A Rare Case Report." Medical Journal of Dr. D.Y. Patil Vidyapeeth 17, Suppl 2 (2024): S374—S376. http://dx.doi.org/10.4103/mjdrdypu.mjdrdypu_102_24.

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ABSTRACT Pulmonary osseous metaplasia is the term used to describe the formation of mature bone tissue inside the lung parenchyma. It is a rare disorder that has been linked to chronic lung diseases such as bronchiectasis, pneumonia, and pulmonary fibrosis. Disseminated ossification of the lung is mostly related to two patterns namely dendriform and nodular. It is a postmortem discovery that is extremely uncommon in living people. A 41-year-old man with pulmonary osseous metaplasia is the subject of our current study. Lung transplantation was performed on the patient, who had history of type I
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Ahmed, Fatima H., Sarah Abdelrahman, and Ahmed Ibrahim. "Primary Osseous Metaplasia of Right Breast." Open Journal of Pathology 10, no. 03 (2020): 108–12. http://dx.doi.org/10.4236/ojpathology.2020.103010.

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Kriplani, Divya, Priti P. Trivedi, and Manoj J. Shah. "Renal Cell Carcinoma with Osseous Metaplasia." Journal of Case Reports 3, no. 1 (2013): 165–68. http://dx.doi.org/10.17659/01.2013.0040.

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White, Justin, Joanne Hickey, Donna Gilmour, and Afshin Ansari. "Endometrial osseous metaplasia with secondary infertility." Canadian Medical Association Journal 194, no. 25 (2022): E868—E869. http://dx.doi.org/10.1503/cmaj.220183.

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Cochrane-Davis, Lucia, and Afaq Khan. "Osseous metaplasia of a thyroid nodule." Pathology 53 (July 2021): S24. http://dx.doi.org/10.1016/j.pathol.2021.06.020.

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Hjelkrem, Michael, Ajay Pabby, and Kevin Fair. "Osseous Metaplasia in a Colorectal Neoplasia." American Journal of Gastroenterology 104 (October 2009): S335. http://dx.doi.org/10.14309/00000434-200910003-00908.

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Nakajima, Hitoshi, Satoru Iwane, Takafumi Mikami, et al. "Osseous Metaplasia in Benign Rectal Polyps." Journal of Clinical Gastroenterology 25, no. 3 (1997): 558–59. http://dx.doi.org/10.1097/00004836-199710000-00019.

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Pieczarka, Emily M., Duncan S. Russell, Kelly S. Santangelo, Famke Aeffner, and Mary Jo Burkhard. "Osseous metaplasia within a canine insulinoma." Veterinary Clinical Pathology 43, no. 1 (2014): 89–93. http://dx.doi.org/10.1111/vcp.12117.

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Joshi, M., D. D. Remoundos, F. Ahmed, G. Rees, and G. Cunnick. "An unusual breast lump: osseous metaplasia." Case Reports 2013, feb04 1 (2013): bcr2012008239. http://dx.doi.org/10.1136/bcr-2012-008239.

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Lainas, Trifon, Ioannis Zorzovilis, Georgios Petsas, Efthymia Alexopoulou, Georgios Lainas, and Tasos Ioakimidis. "Osseous metaplasia: Case report and review." Fertility and Sterility 82, no. 5 (2004): 1433–35. http://dx.doi.org/10.1016/j.fertnstert.2004.04.055.

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