| Eponyms in category: Cancer and tumours |
| 175
main and alternative
entries found.
|
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| Abercrombie's tumour (Hutchison's disease) |
| This syndrome consists of a malignant tumor, often metastasing to the liver, lungs, and bones. |
| Abernethy's sarcoma |
| A circumscribed neoplasm consisting of malignant fat cells occurring principally in the trunk. |
| Abrikossoff's myoblastoma |
| Rare, usually benign tumor of the Schwann cells or nerve cells, occurring cutaneously or subcutaneously on any part of the body; also in the skeletal muscles or internal organs. |
| Abrikossoff’s myoblastoma and tumor (Abrikossoff's myoblastoma) |
| Rare, usually benign tumor of the Schwann cells or nerve cells, occurring cutaneously or subcutaneously on any part of the body; also in the skeletal muscles or internal organs. |
| Abrikossoff’s tumor (Abrikossoff's myoblastoma) |
| Rare, usually benign tumor of the Schwann cells or nerve cells, occurring cutaneously or subcutaneously on any part of the body; also in the skeletal muscles or internal organs. |
| Abrikossoff’s tumor of skin (Abrikossoff's myoblastoma) |
| Rare, usually benign tumor of the Schwann cells or nerve cells, occurring cutaneously or subcutaneously on any part of the body; also in the skeletal muscles or internal organs. |
| Ackerman's tumour |
| A rare locally malignant tumor which is malignant in behaviour but whose pathology is relatively benign. |
| Ackermann’s carcinoma (Ackerman's tumour) |
| A rare locally malignant tumor which is malignant in behaviour but whose pathology is relatively benign. |
| Albarran's glands |
| Subtrigonal glands in the bladder.
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| Albrecht-Arzt-Warthin tumour (Warthin's tumour) |
| Benign salivary gland tumour with lymphoid tissue covered by epithelium. |
| Anderson's syndrome |
| Obsolete term for paraneoplastic hypoglycaemia in carcinoma of the adrenal gland. |
| Angiosarcoma Kaposi (Kaposi's sarcoma) |
| A particular form of malign, multifocal vascular neoplasm. |
| Bard's syndrome |
| Eponym used to indicate pulmonary metastases from cancer of the stomach. |
| Barré-Masson syndrome |
| A benign tumor of the glomus body. |
| Barré-Masson tumour (Barré-Masson syndrome) |
| A benign tumor of the glomus body. |
| Bence Jones’ syndrome (Kahler's disease) |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Billroth's disease II |
| Malignant lymphoma. |
| Birch-Hirschfeld syndrome (Wilms' tumour) |
| A highly malignantand rapidly developing tumour of the kidney. |
| Birch-Hirschfeld tumour (Wilms' tumour) |
| A highly malignantand rapidly developing tumour of the kidney. |
| Bonfils' disease (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Bonfils' syndrome (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Bozzolo’s disease (Kahler's disease) |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Brodie's syndrome I |
| Usually benign, rapidly growing tumour of the breast occurring after puberty |
| Brodie’s serocystic disease (Brodie's syndrome I) |
| Usually benign, rapidly growing tumour of the breast occurring after puberty |
| Brodie’s tumour (Brodie's syndrome I) |
| Usually benign, rapidly growing tumour of the breast occurring after puberty |
| Burkitt's lymphoma |
| Malign tumor in facial and maxillary bones. |
| Burkitt's sarcoma (Burkitt's lymphoma) |
| Malign tumor in facial and maxillary bones. |
| Burkitt's syndrome (Burkitt's lymphoma) |
| Malign tumor in facial and maxillary bones. |
| Burkitt's tumour (Burkitt's lymphoma) |
| Malign tumor in facial and maxillary bones. |
| Burkitt’s African lymphoma (Burkitt's lymphoma) |
| Malign tumor in facial and maxillary bones. |
| Buschke-Löwenstein tumour |
| Giant chondyloma - a large warty tumor - of the genital region with expansive, destructive growth. |
| Bäfverstedt syndrome (Spiegler-Fendt sarcoid) |
| A rare form of benign recurrent tumor of the lymphoreticular tissue. |
| Castleman's disease (Castleman's tumour) |
| Unusual mediastinal lymph node hyperplasia resembling thymoma. |
| Castleman's lymphoma (Castleman's tumour) |
| Unusual mediastinal lymph node hyperplasia resembling thymoma. |
| Castleman's tumour |
| Unusual mediastinal lymph node hyperplasia resembling thymoma. |
| Chrobak's symptom |
| A probe sinks deep into necrotic tissue, particularly seen in cervix-carcinoma. |
| Ciuffini-Pancoast syndrome (Pancoast's syndrome) |
| A syndrome characterized by a malignant neoplasm of the cervical area with destructive lesions of the thorax inlet and involvement of the brachial plexus and cervical sympathetic nerves. |
| Ciuffini-Pancoast-Tobías syndrome (Pancoast's syndrome) |
| A syndrome characterized by a malignant neoplasm of the cervical area with destructive lesions of the thorax inlet and involvement of the brachial plexus and cervical sympathetic nerves. |
| Codman's triangle |
| Radiological sign in osteosarcoma. |
| Codman's tumour |
| A benign tumor of the cartilage and cartilage-forming connective tissue, most frequently localized to the epiphyses of the long bones, e.g., femur, humerus, and tibia. |
| Cushing's symphalangism |
| A syndrome of symphalangism with fusion of the midphalangeal joints; fusion of elbow and carpal and tarsal bones; absence of the normal articular folds. |
| Cushing's syndrome II |
| A syndrome of multiple tumours of the spinal nerve roots and auditory nerves. |
| Demons-Meigs syndrome (Meigs' syndrome) |
| A syndrome characterised by a solid ovarian tumour, usually a fibroma, accompanied by ascites and pleural effusion. |
| Denny-Brown's syndrome II |
| Bronchogenic carcinoma associated with primary degeneration of the dorsal root ganglion cells with primary degeneration of the muscles.
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| Denny-Brown’s association (Denny-Brown's syndrome II) |
| Bronchogenic carcinoma associated with primary degeneration of the dorsal root ganglion cells with primary degeneration of the muscles.
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| Denny-Brown’s syndrome I (Denny-Brown's syndrome II) |
| Bronchogenic carcinoma associated with primary degeneration of the dorsal root ganglion cells with primary degeneration of the muscles.
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| Ehrlich's tumour |
| Transplantable tumor originally derived from breast carcinoma in mice. |
| Erdheim's tumour |
| A slow-growing suprasellar neoplasm. |
| Ewing's angioendothelioma (Ewing's sarcoma) |
| A primary tumour in the bone. |
| Ewing's endothelial sarcoma (Ewing's sarcoma) |
| A primary tumour in the bone. |
| Ewing's sarcoma |
| A primary tumour in the bone. |
| Ewing’s syndrome (Ewing's sarcoma) |
| A primary tumour in the bone. |
| Ewing’s tumour (Ewing's sarcoma) |
| A primary tumour in the bone. |
| Extraosseous Ewing's sarcoma |
| Ewing's sarcoma when found entirely restricted to soft tissue.
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| Fibiger's tumour |
| Squamous cell carcinoma of the stomach in the rat caused by larvae of the nematode Spiroptera neoplastica. |
| Foster Kennedy's syndrome (Kennedy's syndrome) |
| Condition characterised by unilateral ipsilateral atrophy with contralateral papilloedema, central scotoma, and anosmia (absence of the sense of smell). |
| Gartner's cyst |
| A term comprising various ovarial tumours that are assumed to have developed in persistent vestiges of mesonephros. |
| Gartner's tumour (Gartner's cyst) |
| A term comprising various ovarial tumours that are assumed to have developed in persistent vestiges of mesonephros. |
| Gorlin-Vickers syndrome (Williams-Pollock syndrome) |
| A familial syndrome characterised by multiple mucosal neuromas, medullary carcinoma of the thyroid gland, and frequently associated with a marfanoid build. Inheritance is autosomal dominant. |
| Gowers-Paton-Kennedy syndrome (Kennedy's syndrome) |
| Condition characterised by unilateral ipsilateral atrophy with contralateral papilloedema, central scotoma, and anosmia (absence of the sense of smell). |
| Hare's syndrome (Pancoast's syndrome) |
| A syndrome characterized by a malignant neoplasm of the cervical area with destructive lesions of the thorax inlet and involvement of the brachial plexus and cervical sympathetic nerves. |
| Hippel's disease (Hippel-Lindau tumour) |
| A disturbance characterised by angiomata of the retina and cysts and angiomata of the brain and certain visceral organs. |
| Hippel-Lindau tumour |
| A disturbance characterised by angiomata of the retina and cysts and angiomata of the brain and certain visceral organs. |
| Hodgkin's disease |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Hodgkin's paragranuloma |
| A more benign form of Hodgkin’s disease with a dominance of lymphatic tissue.
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| Hodgkin's sarcoma |
| A more invasive form of Hodgkin’s disease.
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| Hodgkin-Paltauf-Sternberg disease (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Hodgkin-Paltauf-Sternberg syndrome (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Hodgkin’s granuloma (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Hodgkin’s paragranuloma (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Hodgkin’s syndrome (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Huppert’s disease (Kahler's disease) |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Huppert’s syndrome (Kahler's disease) |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Hutchinson-Weber-Peutz syndrome (Peutz-Jeghers syndrome) |
| Gastrointestinal polyposis associated with benign adenomatous tumours and mucocutaneous pigmentation consisting of discrete brown to bluish-black macules about the lips, oral mucosa, and other facial orifices. |
| Hutchison's disease |
| This syndrome consists of a malignant tumor, often metastasing to the liver, lungs, and bones. |
| Hutchison's syndrome (Hutchison's disease) |
| This syndrome consists of a malignant tumor, often metastasing to the liver, lungs, and bones. |
| Hutchison’s tumour (Hutchison's disease) |
| This syndrome consists of a malignant tumor, often metastasing to the liver, lungs, and bones. |
| Jeghers' syndrome (Peutz-Jeghers syndrome) |
| Gastrointestinal polyposis associated with benign adenomatous tumours and mucocutaneous pigmentation consisting of discrete brown to bluish-black macules about the lips, oral mucosa, and other facial orifices. |
| Kahler's disease |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Kahler's syndrome (Kahler's disease) |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Kahler-Bozzolo disease (Kahler's disease) |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Kaposi haemangiomatosis (Kaposi's sarcoma) |
| A particular form of malign, multifocal vascular neoplasm. |
| Kaposi's angiomatosis (Kaposi's sarcoma) |
| A particular form of malign, multifocal vascular neoplasm. |
| Kaposi's sarcoma |
| A particular form of malign, multifocal vascular neoplasm. |
| Kaposi's sarcomatosis (Kaposi's sarcoma) |
| A particular form of malign, multifocal vascular neoplasm. |
| Kaposi's syndrome (Kaposi's sarcoma) |
| A particular form of malign, multifocal vascular neoplasm. |
| Kaposi-Spiegler sarcomatosis (Spiegler-Fendt sarcoid) |
| A rare form of benign recurrent tumor of the lymphoreticular tissue. |
| Kennedy's phenomenon (Kennedy's syndrome) |
| Condition characterised by unilateral ipsilateral atrophy with contralateral papilloedema, central scotoma, and anosmia (absence of the sense of smell). |
| Kennedy's syndrome |
| Condition characterised by unilateral ipsilateral atrophy with contralateral papilloedema, central scotoma, and anosmia (absence of the sense of smell). |
| Klostermann’s syndrome (Peutz-Jeghers syndrome) |
| Gastrointestinal polyposis associated with benign adenomatous tumours and mucocutaneous pigmentation consisting of discrete brown to bluish-black macules about the lips, oral mucosa, and other facial orifices. |
| Krukenberg's tumour |
| A malignant tumor of the ovary, usually bilateral, with fibromyxomatous stroma and scattered mucin secreting signet cells |
| Krukenberg’s syndrome (Krukenberg's tumour) |
| A malignant tumor of the ovary, usually bilateral, with fibromyxomatous stroma and scattered mucin secreting signet cells |
| Leydig's tumour |
| A rare and usually benign hormone-producing tumour in the testicle originating from Leydig interstitial cells or similar hilu cells in the ovary. |
| Li-Fraumeni syndrome |
| A rare familial syndrome characterized by the occurrence of sarcomas, breast cancer, brain tumours, leukaemia, and adrenocortical tumours in children and young adults. |
| Lindau's tumour (Hippel-Lindau tumour) |
| A disturbance characterised by angiomata of the retina and cysts and angiomata of the brain and certain visceral organs. |
| Lindau-von Hippel disease (Hippel-Lindau tumour) |
| A disturbance characterised by angiomata of the retina and cysts and angiomata of the brain and certain visceral organs. |
| Lynch's syndrome I and II |
| Familial predisposition to colorectal cancer. |
| MacIntyre’s syndrome (Kahler's disease) |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Masson’s tumours (Barré-Masson syndrome) |
| A benign tumor of the glomus body. |
| Meigs' syndrome |
| A syndrome characterised by a solid ovarian tumour, usually a fibroma, accompanied by ascites and pleural effusion. |
| Meigs-Cass syndrome (Meigs' syndrome) |
| A syndrome characterised by a solid ovarian tumour, usually a fibroma, accompanied by ascites and pleural effusion. |
| Neumann's syndrome (Franz Ernst Christian Neumann) |
| Muscle cell tumour in infants. |
| Nygaard-Brown syndrome (Trousseau's syndrome) |
| Historical, no longer commonly used term for venous thrombosis of the upper and lower extremities associated with visceral cancer. |
| Paget's cancer (Paget's nipple disease) |
| A peculiar form of cancer of the breast gland, beginning as an eczematous condition around areola. |
| Paget's carcinoma (Paget's nipple disease) |
| A peculiar form of cancer of the breast gland, beginning as an eczematous condition around areola. |
| Paget's disease of skin (Paget's extramammary disease) |
| A rare, malign cancer of the skin involving the same cells as the nipple disease. |
| Paget's extramammary disease |
| A rare, malign cancer of the skin involving the same cells as the nipple disease. |
| Paget's nipple (Paget's nipple disease) |
| A peculiar form of cancer of the breast gland, beginning as an eczematous condition around areola. |
| Paget's nipple disease |
| A peculiar form of cancer of the breast gland, beginning as an eczematous condition around areola. |
| Paltauf-Sternberg disease (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Pancoast's apex syndrome (Pancoast's syndrome) |
| A syndrome characterized by a malignant neoplasm of the cervical area with destructive lesions of the thorax inlet and involvement of the brachial plexus and cervical sympathetic nerves. |
| Pancoast's disease (Pancoast's syndrome) |
| A syndrome characterized by a malignant neoplasm of the cervical area with destructive lesions of the thorax inlet and involvement of the brachial plexus and cervical sympathetic nerves. |
| Pancoast's pain syndrome (Pancoast's syndrome) |
| A syndrome characterized by a malignant neoplasm of the cervical area with destructive lesions of the thorax inlet and involvement of the brachial plexus and cervical sympathetic nerves. |
| Pancoast's syndrome |
| A syndrome characterized by a malignant neoplasm of the cervical area with destructive lesions of the thorax inlet and involvement of the brachial plexus and cervical sympathetic nerves. |
| Pancoast's tumour |
| Carcinoma of the apex of the lung. |
| Pancoast-Tobías syndrome (Pancoast's syndrome) |
| A syndrome characterized by a malignant neoplasm of the cervical area with destructive lesions of the thorax inlet and involvement of the brachial plexus and cervical sympathetic nerves. |
| Pap smear (Papanicolaou's smear) |
| Cytodiagnostic test for early detection of cervical cancer. |
| Papanicolaou's smear |
| Cytodiagnostic test for early detection of cervical cancer. |
| Papanicolaou's smear test (Papanicolaou's test) |
| A test for early diagnosis of cervical cancer. |
| Papanicolaou's test |
| A test for early diagnosis of cervical cancer. |
| Parker's syndrome (Hutchison's disease) |
| This syndrome consists of a malignant tumor, often metastasing to the liver, lungs, and bones. |
| Pel-Ebstein fever (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Pepper’s disease (Hutchison's disease) |
| This syndrome consists of a malignant tumor, often metastasing to the liver, lungs, and bones. |
| Peutz-Jeghers hamartosis (Peutz-Jeghers syndrome) |
| Gastrointestinal polyposis associated with benign adenomatous tumours and mucocutaneous pigmentation consisting of discrete brown to bluish-black macules about the lips, oral mucosa, and other facial orifices. |
| Peutz-Jeghers syndrome |
| Gastrointestinal polyposis associated with benign adenomatous tumours and mucocutaneous pigmentation consisting of discrete brown to bluish-black macules about the lips, oral mucosa, and other facial orifices. |
| Peutz-Klostermann syndrome (Peutz-Jeghers syndrome) |
| Gastrointestinal polyposis associated with benign adenomatous tumours and mucocutaneous pigmentation consisting of discrete brown to bluish-black macules about the lips, oral mucosa, and other facial orifices. |
| Peutz-Touraine syndrome (Peutz-Jeghers syndrome) |
| Gastrointestinal polyposis associated with benign adenomatous tumours and mucocutaneous pigmentation consisting of discrete brown to bluish-black macules about the lips, oral mucosa, and other facial orifices. |
| Peutz-Touraine-Jeghers syndrome (Peutz-Jeghers syndrome) |
| Gastrointestinal polyposis associated with benign adenomatous tumours and mucocutaneous pigmentation consisting of discrete brown to bluish-black macules about the lips, oral mucosa, and other facial orifices. |
| Peutz’ syndrome (Peutz-Jeghers syndrome) |
| Gastrointestinal polyposis associated with benign adenomatous tumours and mucocutaneous pigmentation consisting of discrete brown to bluish-black macules about the lips, oral mucosa, and other facial orifices. |
| Pott's cancer |
| Coal tar-induced cancer of the skin particularly localized to the scrotum. |
| Razdolskii's syndrome |
| Pressure on the spinal cord induced by extramedullar tumour originated after lumbal punction |
| Recklinhausen's tumour |
| An adenoleiomyofibroma on wall of the fallopian tube or posterior uterine wall.
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| Roser-Braun symptom |
| Absence of pulsation of the dura in a trephination opening suggests an underlying tumour. |
| Rustitskii’s disease (Kahler's disease) |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Schauta-Amreich operation |
| An improvement of Schauta's technique for treatment of cervical and endometrial carcinomas. |
| Schauta-Stoeckel operation |
| Vaginal radical extirpation for early stages of cancer colli uteri. |
| Schiller's test |
| Test for carcinoma of the cervix. |
| Schmincke-Regaud tumour |
| An undifferentiated lymhoepithelial carcinoma that originates in the nasopharynx and metastases to the lymph nodes. |
| Schridde's cancer hair |
| Thick, lacklustre dark hairs found in the beard and on the temple of cancerous or cachectic patients. |
| Sensory neuropathy type Denny-Brown (Denny-Brown's syndrome II) |
| Bronchogenic carcinoma associated with primary degeneration of the dorsal root ganglion cells with primary degeneration of the muscles.
|
| Sertoli's cell tumour |
| A rare form of tumour originating from Sertoli cells. |
| Sertoli-Leydig cell tumour (Sertoli's cell tumour) |
| A rare form of tumour originating from Sertoli cells. |
| Sertoli-Leydig cell tumour (Leydig's tumour) |
| A rare and usually benign hormone-producing tumour in the testicle originating from Leydig interstitial cells or similar hilu cells in the ovary. |
| Sipple's syndrome |
| A neoplastic disease, characterized by a triad of medullary thyroid carcinoma, pheochromocytoma, and parathyroid hyperplasia or adenoma, in association with elevated calcitonin and catecholamine levels. |
| Smith’s syndrome (Hutchison's disease) |
| This syndrome consists of a malignant tumor, often metastasing to the liver, lungs, and bones. |
| Spegelberg's sign |
| A diagnostic sign for early recognition of collum carcinoma of the uterus with the mucosa still intact. |
| Spiegelberg's sign of carcinoma (Spegelberg's sign) |
| A diagnostic sign for early recognition of collum carcinoma of the uterus with the mucosa still intact. |
| Spiegler-Fendt sarcoid |
| A rare form of benign recurrent tumor of the lymphoreticular tissue. |
| Spiegler-Fendt sarcomatosis (Spiegler-Fendt sarcoid) |
| A rare form of benign recurrent tumor of the lymphoreticular tissue. |
| Sternberg’s disease (Hodgkin's disease) |
| A neoplastic disease of unknown aetiology, considered to be a form of malignant lymphoma, producing enlargement of lymphoid tissue, spleen, and liver with invasion of other tissues. |
| Tobías' syndrome (Pancoast's syndrome) |
| A syndrome characterized by a malignant neoplasm of the cervical area with destructive lesions of the thorax inlet and involvement of the brachial plexus and cervical sympathetic nerves. |
| Troisier's node or sign (Virchow's node) |
| Enlargement of one of the supraclavicular lymph nodes. |
| Trousseau's phenomenon (Trousseau's syndrome) |
| Historical, no longer commonly used term for venous thrombosis of the upper and lower extremities associated with visceral cancer. |
| Trousseau's syndrome |
| Historical, no longer commonly used term for venous thrombosis of the upper and lower extremities associated with visceral cancer. |
| Vessel’s syndrome (Cushing's symphalangism) |
| A syndrome of symphalangism with fusion of the midphalangeal joints; fusion of elbow and carpal and tarsal bones; absence of the normal articular folds. |
| Virchow's gland (Virchow's node) |
| Enlargement of one of the supraclavicular lymph nodes. |
| Virchow's node |
| Enlargement of one of the supraclavicular lymph nodes. |
| von Hippel-Lindau tumour (Hippel-Lindau tumour) |
| A disturbance characterised by angiomata of the retina and cysts and angiomata of the brain and certain visceral organs. |
| von Recklinghausen's tumour (Recklinhausen's tumour) |
| An adenoleiomyofibroma on wall of the fallopian tube or posterior uterine wall.
|
| von Rustitskii’s syndrome (Kahler's disease) |
| A fatal condition with occurrence of multiple malign tumours disease (multiple myeloma) in the bone marrow, causing disturbances of its function. |
| Warthin's tumour |
| Benign salivary gland tumour with lymphoid tissue covered by epithelium. |
| Watkins-Schauta-Wertheim operation (Wertheim's operation) |
| An improved type of radical abdominal hysterectomy introduced in 1900. |
| Wermer's syndrome |
| An inherited genetic defect that produces hyperplasia or malignant tumours in several endocrine glands. |
| Wertheim's operation |
| An improved type of radical abdominal hysterectomy introduced in 1900. |
| Wertheim-Meigs operation (Wertheim's operation) |
| An improved type of radical abdominal hysterectomy introduced in 1900. |
| Wertheim-Schauta operation (Wertheim's operation) |
| An improved type of radical abdominal hysterectomy introduced in 1900. |
| Williams-Pollock syndrome |
| A familial syndrome characterised by multiple mucosal neuromas, medullary carcinoma of the thyroid gland, and frequently associated with a marfanoid build. Inheritance is autosomal dominant. |
| Wilms Kopfhöcker (German) (Wilms' cones) |
| Cones on the interior wall of dermoid cysts and teratoma. Embryonal. |
| Wilms nephroblastom (Wilms' tumour) |
| A highly malignantand rapidly developing tumour of the kidney. |
| Wilms' cones |
| Cones on the interior wall of dermoid cysts and teratoma. Embryonal. |
| Wilms' syndrome (Wilms' tumour) |
| A highly malignantand rapidly developing tumour of the kidney. |
| Wilms' tumour |
| A highly malignantand rapidly developing tumour of the kidney. |
| Wilmsche Zotte (German) (Wilms' cones) |
| Cones on the interior wall of dermoid cysts and teratoma. Embryonal. |
| Winer's dilated pore |
| A hair structure anomaly that appears as an enlarged solitary comedo, most commonly on the face, predominantly on the upper lip, cheek, or forehead of a middle-aged person |
| Winer’s pore (Winer's dilated pore) |
| A hair structure anomaly that appears as an enlarged solitary comedo, most commonly on the face, predominantly on the upper lip, cheek, or forehead of a middle-aged person |
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