Primary extramedullary plasmacytoma of the parotid gland: a case report and review of the literature

1998 ◽  
Vol 112 (2) ◽  
pp. 179-181 ◽  
Author(s):  
J. Gonzalez-Garcia ◽  
K. Ghufoor ◽  
G. Sandhu ◽  
P. A. Thorpe ◽  
J. Hadley
Keyword(s):  
Parotid Gland ◽  
Rare Condition ◽  
Surgical Excision ◽  
Good Prognosis ◽  
Extramedullary Plasmacytoma ◽  
Treatment Modalities ◽  
Malignant Neoplasms ◽  
Upper Respiratory Tract ◽  
Review Of The Literature ◽  
The Right

AbstractSolitary extramedullary plasmacytomas are uncommon malignant neoplasms with a great predilection for the upper respiratory tract. Extramedullary plasmacytoma involving the parotid gland is an extremely rare condition. This report describes the case of a primary extramedullary plasmacytoma arising in the right parotid gland of a 63-year-old man. A review of the literature reveals that this disease has generally a good prognosis, provided that multiple myeloma has been excluded. The treatment of choice should be surgical excision followed by radiotherapy, although from this study there is insufficient evidence to suggest that this is more effective than surgery alone. All patients must have regular long-term follow-up to monitor for recurrence or dissemination, in which event chemotherapy may be considered in addition to the other treatment modalities.

scholarly journals Congenital Unilateral Agenesis of the Parotid Gland: A Case Report and Review of the Literature

2016 ◽  
Vol 2016 ◽  
pp. 1-5
Author(s):  
Afshin Teymoortash ◽  
Stephan Hoch
Keyword(s):  
Case Report ◽  
Parotid Gland ◽  
Rare Condition ◽  
Clinicopathological Characteristics ◽  
Review Of The Literature ◽  
The Right ◽  
Left Parotid Gland

Congenital unilateral agenesis of the parotid gland is a rare condition with only few cases reported in the literature. A review of 21 cases in the available literature is presented in this article. We report on a further case of a 34-year-old woman with agenesis of the left parotid gland and lipoma of the right cheek. Clinicopathological characteristics of described cases in the literature were discussed.

scholarly journals Primary Lymphoepithelial-Like Carcinoma of the Parotid Gland- Case Presentation

2018 ◽  
Vol 22 (1) ◽  
pp. 43-48 ◽  
Author(s):  
Athanasios Poulopoulos ◽  
Evangelos Parcharidis ◽  
Christina Nikolaidou ◽  
Aikaterini Aidonopoulou
Keyword(s):  
Salivary Gland ◽  
Parotid Gland ◽  
Ct Scanning ◽  
Surgical Excision ◽  
Excision Biopsy ◽  
Salivary Gland Neoplasm ◽  
Malignant Neoplasms ◽  
Positive Staining ◽  
Individual Variables ◽  
The Right

SummaryBackground/Aim: Primary Lymphoepithelial carcinoma (PLEC) is a rare subtype of salivary gland cancers, which comprises only 0.4% of salivary malignant neoplasms and only a few cases have been presented previously. Case report: A patient with PLEC of the parotid gland, its management and the available literature are presented. A 53-year-old woman with initial lesion of a lump in the region of the right parotid received treatment with antibiotics which did not lead to improvement. MRI was performed that recorded the presence of a tumor in the right parotid gland and the patient subsequently underwent excision biopsy. The histopathological evaluation together with additional immunohistochemical positive staining of EMA+, EGFR+, p63+, CK 5/6+, AE1/AE3+ established the diagnosis of PLEC. A PET-CT scanning has shown nor primary mucosal source neither skin lesion to account for any possible metastatic disease, consequently a course of adjuvant post-operative radiotherapy to the region of the right parotid gland was performed. Conclusions: In the differential diagnosis of a parotid gland lump should be included the possibility of a rare salivary gland neoplasm such as PLEC. Surgical excision and radiotherapy have been proposed for the treatment of early and advanced neoplasm stages. Ages of the patient, stage of the neoplasm as well as type of therapy are significant and individual variables for the prediction of the prognosis.

Rheology of right ventricular outflow tract obstruction: sub-pulmonary membrane developing months after primary intervention to treat pulmonary atresia with intact interventricular septum

2021 ◽  
pp. 1-4
Author(s):  
Baher M. Hanna ◽  
Wesam E. El-Mozy ◽  
Sonia A. El-Saiedi
Keyword(s):  
Right Ventricular ◽  
Interventricular Septum ◽  
Pulmonary Atresia ◽  
Right Ventricular Outflow Tract ◽  
Rare Condition ◽  
Surgical Excision ◽  
Ventricular Outflow Tract ◽  
Outflow Tract ◽  
Ventricular Outflow Tract Obstruction ◽  
The Right

Abstract Isolated sub-pulmonary membrane is a rare condition, the origin of which has been debatable. Transcatheter treatment of pulmonary valve atresia with intact interventricular septum by radiofrequency perforation and balloon dilatation to restore biventricular circulation is gaining more popularity, with improving results over time. We report in our experience of 79 cases in 10 years the development of a sub-pulmonary membrane in 4 cases: causing significant obstruction requiring surgical excision in one case that revealed a fibrous membrane on pathology; causing mild right ventricular outflow tract obstruction in another and not yet causing obstruction in 2. On cardiac MRI, the right ventricular outflow tract and the right ventricular outflow tract/pulmonary atresia angle showed no morphological abnormalities.

scholarly journals An Exceptional Case of Intraparotid Plexiform Neurofibroma Originating from Autonomic Fibers of the Auriculotemporal Nerve

2017 ◽  
Vol 2017 ◽  
pp. 1-5 ◽  
Author(s):  
Sarantis Blioskas ◽  
Sotiris Sotiriou ◽  
Katerina Rizou ◽  
Triantafyllia Koletsa ◽  
Petros Karkos ◽  
...  
Keyword(s):  
Parotid Gland ◽  
Plexiform Neurofibroma ◽  
Surgical Excision ◽  
Neurofibromatosis Type ◽  
Exceptional Case ◽  
Benign Tumors ◽  
First Case ◽  
Superficial Lobe ◽  
The Right ◽  
Auriculotemporal Nerve

Plexiform neurofibromas are benign tumors that tend to occur in patients suffering from neurofibromatosis type 1 (NF-1). This report addresses a rare case where the tumor affected the parotid gland, deriving almost exclusively from the peripheral portion of the facial nerve. A 6-year-old male was referred to us complaining about a gradually enlarging swelling over the right parotid area. Imaging localized the lesion to the superficial lobe of the parotid gland, suggesting a neurofibroma. Cosmetic disfigurement and a functional deficit led us to perform complete surgical resection. Meticulous surgical dissection as well as auriculotemporal nerve origin made complete extirpation possible with almost zero morbidity and ensured alleviation of both aesthetic impairment and pain. This is the first case of an intraparotid PN in a pediatric NF-1 patient, which originated from branches of the auriculotemporal nerve and particularly from fibers of the autonomic nervous system. Radical surgical excision was decided according to established decision-making algorithms.

scholarly journals Persistent Enlarged Occipital Sinus with Absent Unilateral Transverse Sinus

2019 ◽  
Vol 10 (03) ◽  
pp. 519-521
Author(s):  
Guru Dutta Satyarthee ◽  
Luis Rafael Moscote-Salazar ◽  
Amit Agrawal
Keyword(s):  
Rare Condition ◽  
Surgical Excision ◽  
Transverse Sinus ◽  
Venous Sinus ◽  
Occipital Sinus ◽  
Suboccipital Craniotomy ◽  
Acoustic Schwannoma ◽  
The Right ◽  
Dural Opening ◽  
Selection Of

AbstractThe occipital sinus may occasionally remain patent, but the incidence is extremely low and observed in less than 10% of cases. A persistent patent occipital sinus (POS) may be associated with other venous sinus abnormality. The absence of transverse sinus in association with POS is an extremely rare condition and not reported yet. The neuroradiologist, neurosurgeons, otolaryngologist, and neurologist must be aware of the possible existence of POS and other associated venous sinus anomaly, as its warrants very crucial modification of surgical planning, selection of appropriate approaches, and, additionally, may also critically limit the extent of surgical exposure of target, and may hinder intended extent of surgical excision of tumor and associated possibility of injury to POS, which may produce catastrophic hemorrhage, brain swelling, and neurosurgical morbidity. The authors report a 35-year-old male who underwent suboccipital craniotomy for right-side giant acoustic schwannoma. Following the raising bone flap, a markedly prominent, turgid, occipital sinus was observed, not placed exactly in the midline but deviated to the right side, causing further restraining of dural opening. Surgical nuances and intraoperative difficulty encountered along with pertinent literature is reviewed briefly.

scholarly journals Amyloidoma of the right false vocal cord subsequent to extramedullary plasmacytoma of the left parotid gland.

1988 ◽  
Vol 77 (5) ◽  
pp. 722-725
Author(s):  
Tadashi KANOH ◽  
Teruyuki TAKAMATSU ◽  
Tatsuharu OHNO ◽  
Haruto UCHINO ◽  
Akihiko FUJITA
Keyword(s):  
Parotid Gland ◽  
Vocal Cord ◽  
Extramedullary Plasmacytoma ◽  
The Right ◽  
False Vocal ◽  
Left Parotid Gland

scholarly journals Conjunctival Lymphangioma: A Case Report and Brief Review of the Literature

2012 ◽  
Vol 2012 ◽  
pp. 1-4
Author(s):  
Mariana Seca ◽  
Pedro Borges ◽  
Pedro Reimão ◽  
Miguel Gomes ◽  
Angelina Meireles
Keyword(s):  
Tract Infection ◽  
Respiratory Tract ◽  
Respiratory Tract Infection ◽  
Topical Therapy ◽  
Lymphatic Vessels ◽  
Rare Condition ◽  
Upper Respiratory Tract Infection ◽  
Upper Respiratory Tract ◽  
Review Of The Literature ◽  
Upper Respiratory

Background. Lymphangioma is a rare venolymphatic lesion, characterized by dilation of lymphatic vessels. It may occur as an isolated lesion or, more often, represent the surface component of a deep orbital lymphangioma.Case. We report a case of a conjunctival lymphangioma on a 58-year-old male that had simultaneously an upper respiratory tract infection. Excision and biopsy confirmed the nature of the lesion, and there has been no relapse to date.Conclusion. Conjunctival lymphangioma is a rare condition in which the diagnose, must be kept in mind in patients with a red eye resistance to topical therapy and in association with an upper respiratory tract infection. Finally, it is also necessary to be aware of possible recurrence of the lesion.

Isolated extramedullary plasmacytoma of the true vocal fold

2000 ◽  
Vol 114 (7) ◽  
pp. 540-542 ◽  
Author(s):  
Yoseph Rakover ◽  
Michael Bennett ◽  
Rephael David ◽  
Gabriel Rosen
Keyword(s):  
Vocal Fold ◽  
Plasma Cells ◽  
Surgical Excision ◽  
Extramedullary Plasmacytoma ◽  
Light Chains ◽  
History Of ◽  
Kappa Light Chains ◽  
One Year ◽  
The Right ◽  
Local Surgical Excision

We report a rare case of isolated extramedullary plasmacytoma (EMP) of the right true vocal fold in a 38-year-old male with a one-year history of hoarseness. Immunohistochemical staining of plasma cells in the tumour, showed over 90 per cent of them to be positive for kappa light chains. After two attempts at local surgical excision and recurrence within 10 months, the tumour was irradiated.Only seven reported cases of isolated EMP of the true vocal fold are reported in the literature. The therapeutic options are discussed.

scholarly journals Ectopic Compound Odontoma in the Buccal Mucosa: Report of a Rare Case

2015 ◽  
Vol 2015 ◽  
pp. 1-4
Author(s):  
Aparna Venigalla ◽  
Leela Krishna Guttikonda ◽  
Hasini Nelakurthi ◽  
Suresh Babburi ◽  
Soujanya Pinisetti ◽  
...  
Keyword(s):  
Soft Tissue ◽  
Buccal Mucosa ◽  
Rare Case ◽  
Rare Condition ◽  
Histopathologic Examination ◽  
Review Of The Literature ◽  
Girl Child ◽  
The Right ◽  
Compound Odontoma

Eruption of tooth into extraosseous locations is an extremely rare condition. We report a case of a six-year-old girl child with tooth-like structure erupting from the right buccal mucosa. Clinical, radiographic, and histopathologic examination suggested the diagnosis of compound odontoma. Very few cases have been reported so far, where tooth has been located completely in the soft tissue and a variety of names have been used for that condition. A brief review of the literature and the ambiguity in naming the situation is discussed.

Malignant myoepithelioma of the parotid gland: case report and review of the literature

1995 ◽  
Vol 109 (10) ◽  
pp. 995-998 ◽  
Author(s):  
Thomas R. Klumpp ◽  
Rose M. Mohr ◽  
Craig L. Silverman ◽  
Chik-Kwun Tang ◽  
I. B. Elfenbein ◽  
...  
Keyword(s):  
Radiation Therapy ◽  
Parotid Gland ◽  
Progressive Disease ◽  
Surgical Excision ◽  
Combined Modality Treatment ◽  
Adjuvant Radiation ◽  
Rare Tumour ◽  
Diagnostic Biopsy ◽  
Metastatic Sites ◽  
The Right

AbstractA 62-year-old male with a myoepithelioma of the right parotid gland was treated with surgical excision followed by adjuvant radiation therapy. Prior to the completion of radiation therapy, the patient developed progressive disease at local, regional, and distant metastatic sites. Combined modality treatment with radiation and chemotherapy resulted in a significant but transient shrinkage of the tumours at all sites. The patient succumbed to metastatic disease 212 days following the diagnostic biopsy. This case illustrates several of the distinctive clinical and pathological characteristics of this rare tumour.

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