scholarly journals A rare case of accessory maxilla: a case report and literature review of Tessier no. 7 clefts

2020 ◽  
Vol 48 (5) ◽  
pp. 030006052092568
Author(s):  
Ming Sun ◽  
Na Lv ◽  
Ya Xiao ◽  
Jiabin Li ◽  
Guangzhao Guan
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Rare Case ◽  
Clinical Presentation ◽  
Craniofacial Abnormalities ◽  
Supernumerary Teeth ◽  
Computed Tomography Images ◽  
Facial Clefts ◽  
Patient Prognosis ◽  
Patient’S History

Bilateral Tessier no. 7 clefts are rarely reported in the literature. Here, we describe the presence of accessory maxilla with supernumerary teeth in a patient who exhibited bilateral Tessier no. 7 clefts; the diagnosis was established based on the patient’s history, clinical presentation, and computed tomography images. A review of the available literature revealed 24 patients with Tessier no. 7 clefts from 2000 to 2020, including our patient. The most common clinical manifestation in patients with Tessier no. 7 clefts comprises bilateral facial clefts. Additionally, Tessier no. 7 clefts are more frequently found in boys or men, rather than in girls or women. The presence of an accessory maxilla with supernumerary teeth in a patient with bilateral Tessier no. 7 clefts is extremely rare. Early detection of craniofacial abnormalities is important, because it may influence patient prognosis and management.

scholarly journals A Rare Case of Multiple Oblique Facial Clefts with Supernumerary Teeth: Case Report

2012 ◽  
Vol 5 (4) ◽  
pp. 239-242 ◽  
Author(s):  
Manikandhan Ramanathan ◽  
Ananthnarayanan Parameswaran ◽  
Naveen Jayakumar ◽  
Pendem Sneha ◽  
H.F. Sailer
Keyword(s):  
Case Report ◽  
Congenital Anomalies ◽  
Rare Case ◽  
Clinical Presentation ◽  
Craniofacial Anomalies ◽  
Supernumerary Teeth ◽  
Dental Lamina ◽  
Facial Clefts ◽  
Comprehensive Rehabilitation ◽  
High Degree

Oblique facial clefts are rare congenital anomalies that can present alone or in association with other craniofacial anomalies. A high degree of clefting in the embryo may lead to hyperdontia secondary to dichotomy of the dental lamina. Multiple facial clefts with hyperdontia are clinically challenging and demand comprehensive rehabilitation. This article reports a case of multiple oblique facial clefts of variable severity with multiple supernumerary teeth in a 12-year-old boy. The varied clinical presentation along with the rarity of the occurrence mandate documentation.

Spontaneous Osteosarcoma in a Rabbit (Oryctolagus cuniculus)

2007 ◽  
Vol 44 (5) ◽  
pp. 691-694 ◽  
Author(s):  
H. Kondo ◽  
M. Ishikawa ◽  
H. Maeda ◽  
M. Onuma ◽  
M. Masuda ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Oryctolagus Cuniculus ◽  
Rare Case ◽  
Giant Cells ◽  
Helical Computed Tomography ◽  
Multinucleated Giant Cells ◽  
Computed Tomography Images ◽  
Rare Case Report ◽  
The Right

A 6-year-old male cross-breed rabbit ( Oryctolagus cuniculus) was presented with lameness and severe swelling from the right shoulder to brachium. On 16-detector helical computed tomography images of the amputated right forelimb after being fixed in formalin, evident proliferative and destructive lesions of bone were observed. On histologic examination, the tumor was composed of proliferating neoplastic cells that resembled histiocytes, with abundant osteoid production. A large number of multinucleated giant cells were found throughout. This case was diagnosed as osteosarcoma by clinical, radiographic, and histologic findings. This is a rare case report of osteosarcoma in a rabbit consistent with canine predilection sites.

scholarly journals Retroauricular Emphysema as a Late Complication After Bonebridge Implantation: Case Report

2021 ◽  
pp. 014556132110002
Author(s):  
Soňa Šikolová ◽  
Dagmar Hošnová ◽  
Klára Perceová ◽  
Michal Bartoš ◽  
Vít Kruntorád ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Postoperative Complications ◽  
Rare Case ◽  
Late Complication ◽  
Bone Conduction ◽  
Computed Tomography Scan ◽  
Artificial Opening ◽  
Low Incidence ◽  
Tomography Scan

Bonebridge (BB) is the first active implantation system for bone conduction that is placed fully under the skin. Experience suggests that BB is characterized by low incidence of postoperative complications. This case report presents a rare case of a 16-year-old girl with incidence of emphysema occurring over the implant 1 year after operation. We performed a computed tomography scan that showed pockets of gas above the floating mass transducer so we provided the revision surgery and sealed the artificial opening with fat from the earlobe and fibrin glue. Since that time, no air has collected in the retroauricular area and the implant has been fully functional.

scholarly journals Inflammatory Pseudotumour of Stomach in an old lady: a rare case report

2020 ◽  
Vol 8 (1) ◽  
Author(s):  
Azhar AH ◽  
Pasha MA ◽  
Hassan S ◽  
Zainal M ◽  
Rashidi A
Keyword(s):  
Case Report ◽  
Solid Tumor ◽  
Rare Case ◽  
Clinical Presentation ◽  
Inflammatory Pseudotumour ◽  
Secondary Neoplasms ◽  
Laboratory Techniques ◽  
Clinical Presentations ◽  
Rare Case Report ◽  
Adults And Children

Inflammatory pseudotumour (IPT) is a rare benign solid tumor in adults and children. The prevalence, etiology and pathogenesis of this condition are still uncertain. Despite the use of modern laboratory techniques and imaging, it is often difficult to make the diagnosis of IPT. Besides, occasionally the nonspecific morphological appearance and clinical presentation of the mass may mimic other more common primary or secondary neoplasms. IPT is commonly encountered in the lung and mediastinum. Other sites include abdomen (liver, pancreas, stomach, omentum), retroperitoneum, pelvis (bladder) and extremities in children. We report a rare case of gastric inflammatory pseudotumour in a 65-year-old female patient. Clinical presentations and its management along with review of literatures are presented.

A RARE CASE REPORT OF SUBDURAL HAEMATOMA WITH ANEMIA APLASTIC

2021 ◽  
Vol 27 (2) ◽  
pp. 124-128
Author(s):  
Feda Anisah Makkiyah ◽  
Rahmah Hida Nurrizka
Keyword(s):  
Case Report ◽  
Aplastic Anemia ◽  
Subdural Hematoma ◽  
Rare Case ◽  
Subdural Haematoma ◽  
Blood Smear ◽  
Clinical Presentation ◽  
Headache Disorder ◽  
Peripheral Blood Smear ◽  
Rare Case Report

Objective and Importance. To illustrate the development of a rare case of spontaneous subdural hematoma (SDH)  secondary to aplastic anemia and conservative treatment of SDH. Clinical Presentation. A 43-year-old male complained of severe progressive headaches that starting from one month ago. His laboratory values showed pancytopenia and his peripheral blood smear showed no abnormalities except lack of the number of erythrocytes, leukocyte, and thrombocyte and we could not find any malignancy in the smear. He experienced headache,  disorder of balance and decrease of consciousness  CT imaging of the head showed  a 7.0 cm (2 cm thickness) left frontal-parietal subdural hematoma. Conclusion. Aplastic anemia is a rare case with manifested of subdural hematoma.

Occurrence of bilaterally impacted mandibular supernumerary teeth: A rare case report and review of literature

2016 ◽  
Vol 7 (3) ◽  
pp. 198
Author(s):  
PraveshKumar Jhingta ◽  
VinayKumar Bhardwaj ◽  
Deepak Sharma ◽  
Nishant Negi ◽  
Sanjeev Vaid ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Review Of Literature ◽  
Supernumerary Teeth ◽  
Rare Case Report

scholarly journals AGGRESSIVE MESENTRIC FIBROMATOSIS: A RARE CASE REPORT AND REVIEW OF LITERATURE

2013 ◽  
Vol 03 (01) ◽  
pp. 79-82
Author(s):  
Rohan Shetty ◽  
Shubha Bhat ◽  
Rajesh Ballal ◽  
Pramod Makannavar ◽  
Anil Kumar K. N.
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Clinical Presentation ◽  
Aggressive Fibromatosis ◽  
Definitive Diagnosis ◽  
Review Of Literature ◽  
Therapeutic Challenge ◽  
Rare Case Report ◽  
Small Intestinal

AbstractMesentric fibromatosis is a proliferative fibroblastic neoplasm of the small intestinal mesentery with varied clinical presentation. Giant mesentric fibromatosis is uncommon and its rarity poses a diagnostic and therapeutic challenge. This paper presents a recurrent aggressive fibromatosis in a 38 year old male patient, who had initially undergone a laparotomy outside for mass abdomen but only pus was evacuated and definitive diagnosis was not made.

scholarly journals A Rare Case of Osteomyelitis Caused by Haemophilus Parainfluenzae

2017 ◽  
Vol 2 (2) ◽  
pp. 104-106 ◽  
Author(s):  
Fernando Cobo ◽  
Gemma Jiménez ◽  
Javier Rodríguez-Granger ◽  
Antonio Sampedro ◽  
Luis Aliaga-Martínez
Keyword(s):  
Computed Tomography ◽  
Rare Case ◽  
Surrounding Tissue ◽  
Surgical Drainage ◽  
Joint Infections ◽  
Computed Tomography Images ◽  
Haemophilus Parainfluenzae ◽  
Bone Biopsies ◽  
History Of ◽  
History Of Pain

Abstract. Haemophilus parainfluenzae is a rare cause of bone and joint infections. We report a case of calcaneal osteomyelitis due to this microorganism with a review of all published. A 23-year-old woman presented with a 1-month history of pain and inflammation in the calcaneus area. Osteomyelitis was suspected at this location based on computed tomography images. Culture of six bone biopsies and surrounding tissue resulted in the isolation of H. parainfluenzae. Surgical drainage and debridement was performed, and antibiotic treatment was prescribed, resolving the infection.

scholarly journals A rare case of a maxillary fourth molar: Case report

2019 ◽  
Vol 29 (1) ◽  
pp. 125-128
Author(s):  
Valdelias Xavier Pereira ◽  
Alan Patricio Da Silva ◽  
Juliana Spat Carlesso ◽  
Marcelo Ferraz Campos
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Tooth Extraction ◽  
Clinical Case ◽  
Supernumerary Teeth ◽  
Impacted Tooth ◽  
X Ray ◽  
Dental Anomaly ◽  
Molar Teeth ◽  
Distomolar Teeth

Introduction: The objective of this clinical case report is to describe the presence of bilateral fourth molars. The occurrence of supernumerary teeth (ST) is a relatively unusual dental anomaly., It is even more unusual to find patients with distomolar teeth also denominated fourth molar teeth. Presentation of the case: This article describes a clinical case of a 24-year-old patient presenting with a maxillary fourth molar, who was diagnosed by dental x-ray, and surgical resolution of the case. Conclusion: Tooth extraction surgery was the clinical procedure chosen to treat the impacted tooth.

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