Adenocarcinoma of the submandibular gland with positive serum and tissue immunohistochemical staining for both CEA and CA 125: report of a case

1994 ◽  
Vol 108 (8) ◽  
pp. 719-721
Author(s):  
Yoshio Kasuga ◽  
Atsushi Nakai ◽  
Yuji Matsunaga ◽  
Makoto Toi ◽  
Hirohisa Goto ◽  
...  
Keyword(s):  
Submandibular Gland ◽  
Immunohistochemical Staining ◽  
Rare Case ◽  
Ca 125 ◽  
Positive Serum

AbstractA rare case of adenocarcinoma of the submandibular gland with positive serum measurements and tissue immunohistochemical stainings for both CEA and CA 125 is presented.

scholarly journals Management of uterine cystic adenomyosis by laparoscopic surgery: case report

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Cheng-Zhi Zhao ◽  
Bin Wang ◽  
Chun-yan Zhong ◽  
Shen-tao Lu ◽  
Li Lei
Keyword(s):  
Laparoscopic Surgery ◽  
Rare Case ◽  
Cystic Lesion ◽  
Ultrasound Examination ◽  
Ca 125 ◽  
Cystic Lesions ◽  
Good Recovery ◽  
Case Presentation ◽  
Solid Lesions ◽  
Uterine Body

Abstract Background Endometriosis of the uterine body can be manifested as diffuse solid lesions or cystic lesions. The former is common, while the latter is rare, especially for cystic adenomyosis larger than 5 cm. Case presentation A 30-year-old woman was admitted for severe and worsening dysmenorrhea. Ultrasound examination revealed a rare well-circumscribed cystic lesion about 5.5 × 4 × 5.0 cm. CA-125 level was slightly elevated. She accepted laparoscopic surgery and the adenomyotic tissues were excised. The histopathology of the specimen demonstrated the endometrial glands in the walls of cysts and an area of extensive hemorrhage can be seen in the inner wall of cyst. The patient made a good recovery after surgery and her symptoms complete resoluted. Conclusions This is a rare case of a cystic adenomyotic lesion that was treated by laparoscopic surgery.

scholarly journals A rare case of primary tuberculosis of the submandibular gland!!!

2015 ◽  
Vol 16 (1) ◽  
pp. 87-89
Author(s):  
Kasim S. Kasim ◽  
Ebrahim Namavar ◽  
Mohd Razif Mohamad Yunus
Keyword(s):  
Submandibular Gland ◽  
Rare Case ◽  
Primary Tuberculosis

Spontaneous Discharged Submandibular Gland Duct Sialolith: Α Rare Case Report

2019 ◽  
Vol 82 (2) ◽  
pp. 205-207
Author(s):  
Wentao Zhang ◽  
Kai Wang ◽  
Fan Yang
Keyword(s):  
Case Report ◽  
Submandibular Gland ◽  
Rare Case ◽  
Rare Case Report ◽  
Gland Duct

scholarly journals A case of secretory carcinoma of the submandibular gland with unusual immunohistochemical staining

2020 ◽  
Vol 8 (8) ◽  
pp. 1530-1533
Author(s):  
Alexander Karabachev ◽  
Ricardo Aulet ◽  
Mirabelle Sajisevi ◽  
Allison Ciolino
Keyword(s):  
Submandibular Gland ◽  
Immunohistochemical Staining ◽  
Secretory Carcinoma

scholarly journals A rare case of plexiform schwannoma of the lower lip: Treatment and management

2015 ◽  
Vol 48 (02) ◽  
pp. 208-211 ◽  
Author(s):  
Subha Dhua
Keyword(s):  
Immunohistochemical Staining ◽  
Rare Case ◽  
Protein A ◽  
Complete Recovery ◽  
Cystic Degeneration ◽  
Lower Lip ◽  
Plexiform Schwannoma ◽  
S 100 ◽  
Mitotic Figures ◽  
Immunohistochemical Studies

ABSTRACTAn 18-year-old female presented with a swelling on the lower lip, which was insidious in onset and gradually progressive. The mass was completely excised under local anaesthesia. Complete histopathologic and immunohistochemical studies were conducted. The Antoni A areas were found along with typical verocay bodies composed of palisading nuclei and surrounding spaces filled with eosinophilic filaments. No necrosis was noted and there were no atypical mitotic figures. In the Antoni B region, a closely textured matrix with areas of edema, myxomatous changes, cystic degeneration and dilated vessels were noted. On the basis of the histopathologic and immunohistochemical staining with S-100 protein, a diagnosis of plexiform schwannoma was made and has been reported in this study. The post-operative view confirmed complete recovery after 6 weeks of surgery. This is a rare case with the tumour located in the lower lip, as very few cases have been reported in literature and it may be the first one reported from India.

scholarly journals A Rare Case of Myeloid Sarcoma Presenting as an Anorectal Ulcer

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Laxmi Parsa ◽  
Priti Bijpuria ◽  
Daniel Ringold ◽  
David Stein
Keyword(s):  
Immunohistochemical Staining ◽  
Myeloid Leukemia ◽  
Rare Case ◽  
Soft Tissues ◽  
Histochemical Staining ◽  
Myeloid Sarcoma ◽  
Atypical Presentation ◽  
Rare Tumor ◽  
Gastrointestinal Complaint ◽  
Acute Myeloid

Myeloid Sarcoma is a rare tumor composed of myeloblasts occurring at an extramedullary site like bones, or various soft tissues. Myeloid sarcoma may involve the gastrointestinal tract very rarely either solitarily, or occurring simultaneously with acute myeloid leukemia. Its diagnosis is challenging and needs biopsy and immunohistochemical staining. We are describing a case of myeloid sarcoma which presented as a painful anal ulcer mimicking an atypical fissure. Its appearance resembled crohn’s disease on sigmoidoscopy. A biopsy of the ulcer along with histochemical staining led to the diagnosis of myeloid sarcoma. Our case demonstrates the need for aggressive evaluation of any common gastrointestinal complaint with an atypical presentation.

scholarly journals Angiomyolipoma with Epithelial Cysts Masquerading as a Cystic Renal Cell Carcinoma

2015 ◽  
Vol 9 (4) ◽  
pp. 209-211
Author(s):  
Andrew Wood ◽  
Fiona Young ◽  
Marie O'Donnell
Keyword(s):  
Renal Cell Carcinoma ◽  
Cell Carcinoma ◽  
Renal Cell ◽  
Immunohistochemical Staining ◽  
Rare Case ◽  
Renal Tumor ◽  
Staining Pattern ◽  
Cystic Renal Cell Carcinoma ◽  
Epithelial Cysts ◽  
Histological Appearance

Angiomyolipoma with epithelial cysts (AMLEC) is a very uncommon renal tumor. AMLEC has a characteristic histological appearance and immunohistochemical staining pattern, knowledge of which should preclude misdiagnosis by pathologists. We present a rare case of an AMLEC which was suspected to be a cystic renal cell carcinoma radiologically. We describe the characteristic immunological staining pattern and ultrastructural features of this lesion and discuss the potential differential diagnoses.

Sign in / Sign up

Export Citation Format

Share Document