scholarly journals Bilateral sternocleidomastoid tumor of infancy: a rare diagnostic dilemma

Author(s):  
Sachin Goel ◽  
Neha Jain ◽  
Ekta Narang ◽  
Suparna Roy

<p class="abstract">Sternocleidomastoid tumor of infancy (STOI) is a common cause of neck mass in the neonatal period. However, STOIs presenting bilaterally is a rare finding in medical literature. We herein report an unusual case of a bilateral STOI in a five-week infant. The child was given physical therapy which consisted of active and passive physical exercises, warm compresses and massage. Within 10 weeks the swellings reduced considerably in size. Bilateral, firm masses are often confused with lymphadenopathy and are inadvertently treated with antibiotics. Hence, STOI should be kept as an important differential diagnosis for neck mass in the neonatal period.</p>

2020 ◽  
Vol 14 (1) ◽  
Author(s):  
Ahmad Al-Mousa ◽  
Mohammad Nour Shashaa ◽  
Mohamad Shadi Alkarrash ◽  
Mohamad Alkhamis ◽  
Lina Ghabreau ◽  
...  

Abstract Background Seminoma is the most common subtype of testicular cancer and occurs most commonly in patients aged 30–49 years, but decreases to a very low level in men in their 60s or older. Case presentation A 90-year-old Syrian man with a 6-year history of an increase in size of his right scrotum, presented to the urological clinic and, on clinical examination, the findings suggested testicular tumor. After orchiectomy and histology results based on microscopic and immunohistochemical examinations, a pure seminoma was diagnosed, so we describe in this case report the second-oldest patient with classical seminoma in the medical literature. Conclusion This case report has been written to focus on the probability of any type of testicular tumor occurring at any age or decade; urologists should consider seminoma as a differential diagnosis with any testicular swelling even in elderly patients.


2014 ◽  
Vol 3 (3) ◽  
Author(s):  
Tae-Kyung Yoo ◽  
Soo-Hong Kim ◽  
Hyun-Young Kim ◽  
Kwi-Won Park

Branchial cleft anomalies are an important differential diagnosis in congenital neck masses in infants. The third and fourth branchial anomalies are rare branchial cleft anomalies, which are hard to differentiate. We report here an uncommon case of the fourth branchial anomaly that was presented as an asymptomatic neck mass in a neonate.


2017 ◽  
Vol 06 (04) ◽  
pp. 252-257
Author(s):  
Tarek Jazaerly ◽  
Stefan Kostadinov ◽  
Salwa Khedr

AbstractWe report an unusual case of fully developed fetal intestinal segment(s) within a nodule on the chorionic plate of the placenta of a 27-year-old female patient at 37 weeks gestation with spontaneous vaginal delivery. Gross examination of the placenta revealed a chorionic plate nodule near the insertion of the umbilical cord, which, upon microscopic evaluation, raised the differential diagnostic possibilities of placental teratoma, vitelline/omphalomesenteric duct anomaly, and intestinal organoid differentiation. We discuss the distinguishing features, morphogenesis, and clinical significance of the aforementioned entities and review the pertinent medical literature.


2009 ◽  
Vol 13 (3) ◽  
pp. 62 ◽  
Author(s):  
D Meerkotter ◽  
S Andronikou

Two young non-lactating females presented with acutely painful breast masses. Sonographic features showed mixed echogenic masses. Core biopsy was non-diagnostic in both and surgical excision revealed infarcted fibroadenomas. Although fibroadenomas are common, they do not commonly infarct and only rarely in non-lactating and non-pregnant females. These two cases highlight the clinical and imaging characteristics of this important differential diagnosis.


1980 ◽  
Vol 88 (3) ◽  
pp. 211-214 ◽  
Author(s):  
Diran O. Mikaelian ◽  
Stuart A. Scherr ◽  
Leopoldo E. Delucca

Primary Ewing's sarcoma of the mandible is an exceedingly rare finding in the practice of otolaryngology. A case of this neoplasm occurring as a parotid mass is presented. It represented a diagnostic dilemma because of its elusive histopathologic findings. The gross and clinical appearances, microscopic findings, differential diagnosis, and prognosis of this neoplasm are discussed.


2003 ◽  
Vol 117 (4) ◽  
pp. 312-313 ◽  
Author(s):  
Daniel M. Kaplan ◽  
Uriel Attal ◽  
Mordechai Kraus

Benign paroxysmal positional vertigo (BPPV) is a common cause of vertigo and may occur following recent head trauma. Bilateral involvement in BPPV is considered rare and has received little attention in the medical literature. We describe an unusual case of bilateral BPPV in a middle-aged woman that presented during a dental implantation, performed with the use of osteotomes. We discuss the diagnostic and therapeutic challenge of this entity.


2005 ◽  
Vol 129 (6) ◽  
pp. 787-789
Author(s):  
Yun Chyi Lin ◽  
Deborah L. Commins ◽  
Alexander N. Fedenko ◽  
Gregory S. Pinsky

Abstract Periosteal osteoblastoma is an extremely rare bone-forming neoplasm located on the surface of cortical bone. Of the fewer than 30 cases of periosteal osteoblastomas found in the literature, 2 have been reported to be located in cranial bone, and these have not been documented in detail with clinical history, radiographic findings, macroscopic features, and microscopic findings. Although the differential diagnoses of periosteal lesions include parosteal and periosteal osteosarcoma, periosteal chondroma and chondrosarcoma, osteochondroma, osteoid osteoma, periostitis ossificans, and myositis ossificans, an important differential diagnosis both radiologically and pathologically of such a lesion in the cranium is meningioma. We report an unusual case of periosteal osteoblastoma located in the frontal cranial bone that was radiologically consistent with a meningioma. The differential diagnosis of metaplastic meningioma with differentiation toward bone is discussed.


2018 ◽  
Vol 26 (1) ◽  
pp. 76-78
Author(s):  
Soumyajit Das ◽  
Subhasish Mukherjee ◽  
Barun Sharma ◽  
Subash Tamang

Introduction Nuchal fibroma or collagenosis nuchae is a rare benign tumour. It is a slow growing neoplasia of unknown etiogenesis, asymptomatic and of variegated histology. They are more common in males but our case was a female patient. The presentation may mimic sarcoma at times. Case Report An unusual case of a very large neck mass in a 62 years old female patient is reported. The growth involved the dorso-cervical region over a period of approximately 8  years but remained asymptomatic. The mass was excised and post excision histopathology was reported as nuchal fibroma. Discussion The case reported is large compared to the usual size of nuchal fibroma. Association with diabetes mellitus and Gardner’s syndrome has been reported in literature. MRI is the imaging of choice to establish the differential diagnosis.


2008 ◽  
Vol 02 (04) ◽  
pp. 291-293 ◽  
Author(s):  
A. Pina Sumer ◽  
Peruze Celenk

ABSTRACTThe palatal mass can pose a difficult diagnostic dilemma for the clinician. In differential diagnosis of the palatal mass, dental causes must be considered because they are so common. The palatal abscess typically represents the palatally directed drainage of an infection of pulpal or periodontal origin. The palatal abscess is often observed in the premolar-molar region and presents as a compressible mass or swelling usually lateral to the midline. This study reports the unusual case of a 5-year-old girl with a palatal abscess adjacent to the midline. (Eur J Dent 2008;2:291-293)


1980 ◽  
Vol 88 (1) ◽  
pp. 34-36 ◽  
Author(s):  
Gordon B. Hughes ◽  
Kathleen A. Damiani ◽  
Sam E. Kinney ◽  
Howard L. Levine

As preoperative assessment of the patient with a neck mass becomes increasingly sophisticated, differential diagnosis of the masses becomes more complex. The following unusual case of massive swelling in the neck as a result of aural cholesteatoma exemplifies best this complexity and the need for careful preoperative planning.


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