case of endothelioma lymphangio-matodes of the cervix uteri. by Hunter Robb

Cover of: case of endothelioma lymphangio-matodes of the cervix uteri. | Hunter Robb

Published in [Philadelphia? .

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  • Cervix uteri -- Cancer -- Cases, clinical reports, statistics

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Pagination8 p.
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Open LibraryOL18974174M

Download case of endothelioma lymphangio-matodes of the cervix uteri.

Discussion. Primary lymphoma of the uterine cervix is a rare malignancy encountered by gynecologic oncologists. Typically, lymphoma arises in lymphatic organs such as the spleen, thymus, or lymph nodes and spreads to other sites (Groszmann and Benacerraf, ).Approximately one third of lymphoma is extranodal in origin and an even smaller number, estimated to be 1 in (% Author: Maureen E.

Roberts, Hope M. Cottrill. Surgery followed by radiation or chemotherapy is the mainstay of treatment. CASE REPORT: We present the case of a year-old woman with recurrent pathological PAP smears of the cervix and a history of chronic lymphatic leukemia 15 years ago.

Colposcopy of the cervix showed no acetowhite lesion and a conization was by: 4. A year-old woman of Asian origin presented with heavy intermenstrual and postcoital bleeding caused by the rare entity of primary non-Hodgkin’s lymphoma of the cervix uteri, with no evidence of disease elsewhere.

Prompt diagnosis by biopsy avoided unnecessary surgery, and instead appropriate treatment with chemoradiotherapy was by: 5. We present the appearances on CT and MRI of a case of non-Hodgkin's lymphoma (NHL) of uterine cervix.

A year-old woman presented with a short history of urinary symptoms and menorrhagia. Previous cervical smears were normal. Clinically, the cervix was replaced by a huge ulcerating mass. Biopsy showed malignant high grade B-cell by:   Primary lymphoma of the uterus and cervix is rarely encountered.

We present two cases of diffuse large B‐cell lymphoma of the cervix and uterus that were treated with R‐CHOP chemotherapy followed by pelvic radiotherapy.

The women are disease Cited by: To elucidate the clinicopathologic features of lymphoepithelioma-like carcinoma (LELC) of the uterine cervix, we examined three Japanese cases.

We collected three cases of LELC of the uterine cervix between and We examined these patients’ clinicopathologic data, Epstein–Barr virus (EBV) and human papilloma virus (HPV) infectious status, and infiltrated lymphocyte population.

Haemangioma of the cervix is an extremely rare benign lesion, and only a few sporadic cases have been reported to date. In the present report we describe a case of Haemangioma of the cervix that was diagnosed in a year-old patient who consulted for post coital bleeding. cervical and one for uterine corpus lymphoma were prepared including information collected from full text and abstracts of eligible cases.

Accordingly, in Tables 1 and 2, we present the cases to date, without those reported in the above mentioned case series. Results The cases collected included cervical and 60 uterine primary NHL.

Cervical endometriosis is usually a retrospective finding on histology. We describe the diverse symptomatology of the disease, wherein a suspicion of diagnosis may be raised. A series of five patients with cervical endometriosis confirmed on histology was identified.

One patient was asymptomatic but examination revealed a mass arising from the cervix. In the extreme cases the cervix and the greater part of the body of the uterus are found outside the vulva.

In less marked cases the cervix is seen presenting at the vaginal orifice as soon as the labia are separated. In other cases the cervix is felt by the vaginal finger resting on the pelvic floor. Here we report the case of a year-old Japanese woman, gravida 2 and parity 2.

She was admitted due to severe atypical genital bleeding caused by uterine cervical cancer. A >mm tumor was detected at the uterine cervix, and no distal metastasis or swallowing of lymph nodes was revealed by magnetic resonance imaging and a computed tomography.

The clinical presentation of carcinoma of the cervix as cervical lymphadenopathy has not been described before. We report a case of this unusual manifestation of cervical cancer. A year-old woman presented to our Head and Neck department with cervical lymphadenopathy.

A positron emission tomography scan revealed the primary tumour to be in the cervix and a cervical biopsy. Case 1. The first case is a 23 year old male with chief complaint of a tumour in the posterior triangle of the neck, which showed a substantial increase in size in the last 9 months.

No associated signs or symptoms, or any trauma history was reported. CT scan of the neck showed images suggestive of a posterior cervical lymphangioma.

the Uterine Cervix. Online J Health Allied Scs. ; 11(1) 2. Komaki R, Cox JD, Hansen RM, Gunn W, Greenberg M. Malignant lymphoma of the uterus and cervix. Cancer ; 3. Vang R, Medeiros LJ, Fuller GN, Sarris AH, Deavers M. Non-Hodgkin’s lymphoma involving the gynecologic tract: a review of 88 cases.

Adv Anat. From through to May,patients with adenocarcinoma of uterine cervix were initially treated which accounted for % of all initially treated cases with cervical carcinoma.

Malignant ly mphoma of the uterine cervix is exceed - ingly rare and is difficult to diagnose by cervical cytology. The current study presents a case of malignant lymphoma of the uterine cervix that was presumptively diagnosed by cervical cancer screening in which the patient had no clinical symp-toms.

Evidence of human papilloma virus infection but lack of Epstein-Barr virus in lymphoepithelioma-like carcinoma of uterine cervix: report of two cases and review of the literature.

Human pathology. Abstract. Acute inflammation of the cervix results from direct infection by nonspecific microorganisms or by secondary invaders. The former group includes streptococci, staphylococci, and enterococci, and infections with these organisms are prone to occur in puerperal infections.

N2 - Three patients with primary malignant lymphoma of the uterine cervix are reported and the literature is reviewed. All of the patients in the current cases presented with irregular menstruation.

Two patients were found to have diffuse histiocytic lymphoma, and one patient had diffuse mixed lymphoma. Selzer F, Nelson HM () Benign papilloma (polypoid tumor) of the cervix uteri in children; report of two cases.

Am J Obstet Gynecol PubMed Google Scholar A case report with immunohistochemical and ultrastructural analysis.

American Journal of Surgical Pathology. 20(2), Costa, Micheal J et al. Glassy cell features in adenosquamous carcinoma of the uterine cervix.

Am J Clin Pathol ; Hachisuga, Toru et al. Glassy cell carcinoma of the endometrium. A case report. Case report. This is a case of cervical lymphangioma detected at 27 weeks of pregnancy. The diagnosis was confirmed after delivery and the tumor was removed surgically. Images 1, 2: The images show a hypoechoic tumor in the cervical region of the fetus representing the large lymphangioma.

the cervical thoracic cystic lymphangioma is sometimes revealing symptom such as the cervical mass as it was the case for our patient; but in 50% of the cases, they are of fortuitous discovery during a lung radiography. The standard radiography shows an opacity of previous or later mediastinal seat which the aspect is not specific.

Zentralbl Gynakol. Jan 15;88(3) [Cervix hypertrophy and elongatio colli in a year old girl]. [Article in German] Holzegel B. 2 cases (20%) of lymphomas had axillary lymph nodes enlarged while 1 (10%) case presented with inguinal lymph node enlargement in addition to cervical lymphadenopathy.

3 cases (30%) had generalised nodal involvement. Only 11 (%) cases had a positive chest X-ray in tubercular lymphadenitis while 40 (%) cases were negative.

Uterine malignant lymphoma (ML) is a rare disease, accounting for approximately % of malignant tumors of the uterus. Diagnosis by cervical smear and normal cervical biopsy is difficult because ML tumor cells develop in the endometrial stroma and cause minimal necrosis.

4 The surgery for diagnosis and treatment often leads to major.Mar., A11 except 7 cases -far advanced and obvious-were confirmed his- tologically; 1 of these (probable mixed tumor of the parotid) is omitted from the series.

Carcin- oma comprised 30 cases (60% of the group): skin, 14; cervix, 5; breast, 3; corpus uteri, 1. Rare cervical cancers are responsible for a minority of cases encountered by a clinician.

However, behavioral patterns, management, and prognosis of certain rare cervical cancers differ from either squamous carcinomas or adenocarcinomas. Here we present a case of a locally advanced cervical tumor as a presentation of an extranodal cervical non-Hodgkin lymphoma (NHL), with a review of the.

INTRODUCTION. Cancer of the uterine cervix has traditionally been staged clinically, but surgical and radiologic evaluation are now part of assigning stage [].Surgical and radiologic staging provide important information that can impact treatment [].However, the International Federation of Gynecology and Obstetrics (FIGO) has determined that clinical staging is preferable for several.

lungs, stomach, skin, uterine cervix, breast, prostate, and the urinary tract [4]. In most cases, lymphoepithelioma-like carcinoma is related to Epstein-Barr virus (EBV), especially in the thymus gland (thymoma with lymphoid hyperplasia), but no association has been reported between lymphoepithelioma-like car-cinoma of the bladder and EBV [5, 6].

Globally, cervical cancer is the fourth most common cancer in women. Here, we report a case of cutaneous lymphangitis carcinomatosa arising from cervical cancer, an extremely rare and treatment-resistant condition. A year-old Japanese woman presented with genital bleeding.

She was diagnosed as having stage IB1 squamous cell cervical cancer and subsequently treated with radiotherapy. Diffuse large B-cell lymphoma of the uterus suspected of having transformed from a marginal zone B-cell lymphoma harboring trisomy a case report and review of the literature.

Int J Clin Exp Pathol 6: 8. Binesh F, Karimi Zarchi M, Vahedian H, Rajabzadeh Y () Primary malignant lymphoma of the uterine cervix. BMJ Case Rep 9. Results: Tuberculosis was found to be the most common cause of cervical Lymphadenopathy in % cases followed by reactive lymphadenitis in % cases, chronic nonspecific lymphadenitis in % cases and metastatic lymphadenopathy in % cases.

Other causes were unknown primary in % cases and non-Hodgkin’s lymphoma in % cases. CASE: Difficulty inserting a catheter suggests an unyielding cervix. A.W. is a year-old nulliparous woman who seeks treatment for persistent irregular vaginal bleeding.

Her physician attempts an endometrial biopsy in the office but is unable to pass the catheter through the internal cervical os. She schedules office hysteroscopy as follow-up. Watkins RG 4th, Reynolds RA, McComb JG, Tolo VT.

Lymphangiomatosis of the spine: two cases requiring surgical intervention. Spine. Feb 1;28(3):E Jea A, McNeil A, Bhatia S, Birchansky S, Sotrel A, Ragheb J, Morrison G.

A rare case of lymphangiomatosis of the craniocervical spine in conjunction with a Chiari I malformation. Here we report a case of lymphangiomatosis of the colon diagnosed by endoscopic ultrasonography (EUS) and a colonoscopy. CASE REPORT. A yr-old woman underwent barium enema examination as part of a medical checkup.

She had been healthy without specific complaints and had no significant past medical or family history. The patient was cm in. Histological, immunohistochemical, FISH and IGH clonality studies in lymphoma like‐lesions of the uterine cervix.

Biopsies of the cervix of Patient 2 showed diffuse infiltration by monomorphic large CD20 + lymphoid cells with prominent nucleoli and a moderate amount of eosinophilic cytoplasm. There was a high proliferative rate and also nuclear p53 staining in larger cells.

Fifty-four women were examined to find out the incidence of lymphoedema after treatment of cancer of the uterine cervix. The women had all had total hysterectomy and excision of the pelvic lymph nodes and 53 had also received radiotherapy. The character and severity of problems experienced by the patients in their daily living were assessed by.

Synonyms: L iver hygroma, lymphangiomatosis or lymphangio-endothelioma. Prevalence: Lymphangiomas occur in 1 per pediatric admissions with a same sex distribution 3.

Once thought to be rare, simple hepatic cyst are now routinely detected in adults with CT, MRI and ultrasound 5. Postirradiation angiosarcoma* D. Goette, Colonel, MC, USA, and Richard L.

Detlefs, Major, MC, USA Presidio of San Francisco, CA A year-old woman developed a cutaneous angiosarcoma of the lower abdomen in the site where she had received radiotherapy for squamous cell carcinoma of the cervix uteri 23 years earlier.

agent of the cervix uteri? Gynecol Obstet Invest7. Zucca E, Conconi A, Pedrinis E, et al: Nongastric marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue. Blood8. Hitchcock S, Ng AK, Fisher DC, et al: Treatment outcome of mucosa-associated lymphoid tissue/marginal zone non-Hodgkin’s lymphoma.Cervical lymphadenopathy in an adult can result from a vast number of conditions.

They include: malignancy metastases from head and neck tumors lymphoma other neoplastic lesions Castleman disease Kaposi sarcoma infection bacterial infec.with advanced cervical cancer. Typical symptoms are bloody vagi-nal discharge or bleeding subsequent to sexual intercourse and un-explained weight loss.

Thus, on the basis of age, patient history, clinical symptoms, and pelvic examination, cervical carcinoma was the most likely diagnosis in our case.

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